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From www.bloodjournal.org by guest on June 15, 2017. For personal use only. Gene By Interaction PHILIP Resulting LEVINE, in Suppression Substance B ELIZABETH RoBINsON, AND Ix ami ATTEMPTS tient. of Italian unusual agglutinin tested. The anti-Tj, revealed I. of antibodies for the ABO locus first described Bombay. In the literature this the propositus and able with the serum by Dr. Bhat.ia failed to react with animal origin (eel secretor (lectin) to react with Bhende anti-H in the saliva and of amti-H with their sera Bhende also et contained anti-H. al.’ suggested that t.o be the easiest facts were, modified as series by result zygous for in the Including dividuals siblings in the in the one and 4 made red ‘s with (-hickens amid the twin the In ram-c allele classical with that. at the theory genes A, the of vam-ieties framework the this of agglu- anti-H cases family, livimig there amid AB() locus “appears of the AB() groups.” Amzel,4 of Hirszfeld amid 0 B, propositus, of and are by formed Complete loss of I-I B. and only individuals produce anti-H. unpublished individuals, also anti-Il seed of apparently a substance homo- group their sera, there am-c now 12 examples, 7 in studied by Parkin9 and 3 siblings in the first. Bombay avail- cells immul)ize(1 l)lant siblings several , study. the female basic published of of imsdividuals kindly A individual, in cells in- () Imidia,* 2 American in Providence, Rhode Island, is a history of cotisamsguimiitv in parents. From the Jersey; the 1)ivision Institute Blood Bamsk fansily. saliva * These and iii the wish Williams accepted of include , to course to Orilmo of Human Roger indel)ted also I) ‘Seiia Study 2, 1955; are blood Immunohematology, the the made They and of Jumly authors smmggestiomis of for Submitted The fl-bus formation present of the living red three patient as w-as allele europaeus.3 with a new such antil)ody of a new’ individuals The variety The serum H substance. of gemses 0,., A and mutated genes could conpletely 1)0th react Watkins5 the with anti-H in in an Irish family family aI)d ai)d same Shiga),2 Ulex compatible from BIIIGGS factors scm-a of these serum, identical to within Morgan of mutations would failed however, of the product in the dysenteriae -ells of the explanatiomi blood of a group from gloup 0, imcidence of authors. serum Sh. OuvE specificity blood, the of the group specificity red anti-H chicken In addition, apparently in rfhe the the normal Group for a group 0, Rh positive pasuffering fiom a kidney ailment, with all rammdomri group 0 bloods high individual of the serum, CELANO, by Bhende ct al.’ in three genotype is i-eferm-ed to as of a fourth failed tiisin donors P., reacted or am)ti-e was excluded. The anti-H characteristic of a rare at with MA1LIXO Blood FALKINBURG to find compatible extraction, Mrs. was found which occurremsce anti-k, as the LEROY of thank the husband the 3 original a ii(1 2 sih)l i rigs General for 1)rs. of pul)lication Ruggero Col. of the cases’, iii the Aimgust of H. 26, and the for Ilhmode New York; and Island. 1955. Elvin Kabat A. amid serologic Crosby Raritami, New University. Providence, Ceppellini Wm. Foundation, Coltmmbia Flospit,al, discussions Lt. Research Variation, niaking genetic valuable for in findings available specimens this of pmopositus. individual fansily 1100 cases st tidied Imv hot st tidied 1my Bhi:i I ia et :il ,8 hare et al , 6 Sini - From www.bloodjournal.org by guest on June 15, 2017. For personal use only. LEVINE ET 1101 AL. in I 0 B 5#{128} Le(a-b+) ii Le(a+b-) 1’! 1 2 le(a-b+) Le(a-b-) 6 Le(ai-b-) Le (a+b-) Le(a4b-) coniplete Shia(hiiig Partial shadiimg Se : secretor 2 Le(a+b-) Ie(a-b+) homozygous = heterozygous ABH se : nonsecretor The All of them ‘l’lieim- anti-il \Vith all the ame JA’’. to m-elu-ts at C l)OsitiVe out I l)e basis foi- the genem’atiomms thee (as well the By implicat The three nature The with 9 examsiples su1)s(-mipt. ion the repom-ted of the lame tem-miss II iii sigmiifyiumg sem’a of Ui, Isloocls iii figure 1 am-c each fm’omn gemie of is l)y factor the the sil)lings, rare 1)loods. 1 along with the and am)t,iLeb. The 3 t.h)e literature) will absence the would then t hei m het.emozygous amid homozygous used as tree for omi 1)lood groups, group 0 1)loods m-eferred 1)e expected as anti- hem be family unusual be anti- of is made. can data C. especially The of H sul)stancc m’epm-esented \Vith) more whi-h figure 37 I)’Sena,7 pm’oduction antibody and data of these at and Iea(tiolis for umiexpe(-ted H substamice. activity Simmons distinct. hi’ the of some in which and iii i-Lem’ retains described pamemits, origimi ant iionsecmet.oms and indicated anti_Lcm ‘‘h’’ with emlvilonment fom- the gene substances teste(1 (leternuning item is pmesemmt.ed (), bloods I ramismmtted as sigmiifi-ant. m’ea(-tiomms as the Or,, highly hypothesis a amid ty)e Le(a+) l)moposituis, mevealed not case Samtgem-,’#{176}the l)( tiff- iionsecmetom 0 ofis)rimig se(-ret.iomi, the geime rare sui)stances t.elnpelat.ure of rare for 0 am)d are gm’oup iii loomis or by of’ the stll(lV l)e -as for ABH of 11-7 of ex(-eptiomt poimited I I aeais A aieai possible Lewis As 1)100(1 1 = of Le(a-b?) iA Ill FIG. Le(a+b-) to as pheno- in the red cells. to (-omstaimt anti-Il. for a rare gemie, (-om)samiguineous parents. The (his(-ussedl below. ami(l Ii wei-e rec-emitly employed of the thami gem)es whi(-h tem-mis O, as the absema-e detem-mimie a phiemiotype of gemie II pm-esence by amid Watkimis the the implies 01’ the pm-esemice It is obvious that imi the family of the logic propem’l ies which appeal t.o violate fim-st (-1111(1 Ill-i mior apparemitly has the I)m’escmlt dommmiamit. iii the pm-operty pliemiotype amid absence iii the presemit Morgan’#{176} to iii- of the H substaml(-e. It shiou.ild be emphasized that discussion the term ‘‘0’’ has no refem’cma-e to ammy gemme, l)ut. it is imitencled to indicate a phemiotype (lefimie(l by the lack of Fl substamiee amid the presence of anti-Il. Imi short, the use du-ate of H substamsee lack of gene both Memideliams B of the on a basis other exhibit sero- h.. propositus, the m-espectively itot chuldremi dem’ived mother of hemedity. laws from Il-fl. The the father second The 11-5 child, From www.bloodjournal.org by guest on June 15, 2017. For personal use only. 1 102 SUPPRESSION OF BLOOI) GROUP TABLE SUBSTANCE B 1 Secretion No.. Age Phenotype Genotype Su,ressor Testsith . nt,- iene _______ ___ ____ - is e Le Phe- typeG6flOtY1)CF -- -b+ I-i . 55 0 00 Xx a Se Se? + 1-2 . 51 B B? Xx a+h- se sese + + 11-1 11-2 11-3 11-4 . 11-5 . 30 B BO X? it-l)+ Se Se? . 29 B BO Xi a-b- Se Se? + . 27 0, BO xx se sel + Oi BO zr se se? + . 27 29 a+btt+1) A, A,O XX t+b- se sese + 11-6 . 26 Oi, BO xx a+b- se Sese + 11-7 . 23 B BO .V ti-b? Se Set mit. 111-1 111-2 * . 5 A,B A,I1 Vx a+b- se sese + . 2 0 00 Xx 1L-I)+ Se Sese + The numbers t Inhibition correspond of nt-not by given in figure 1. saliva. tested. 111-2, is a secretor nonsecretors. of H substance the Furthermore, Le(a-f-) bloods tion of Mendelian In to those anti-Lea are homozygous heredity. addition, the although both second child, for gene Lee, pal-emits 111-2, this is would phemiotypically al-c -) Le(a and if all constitute adult. a third viola- * following significant be mentioned: a. The parents in generation I are b. The identical twins 11-3 and facts coneermiing this i-emnarkable family may first cousins. 11-4 (both the propositus 11-6 have red cells of siblings 11-3, addition anti-H, 11-4, and to c. The individuals do not secrete H and 11-6 but substances choriom’etinitis) from sufferimig anti-A, are in amit.i-B in their sd-a. Le(a+b-); these three as expected do they secrete Lea substance. d. The remaining siblings lI-i, 11-2, and 11-7 are B, group and se(-Ietors, Lea negative. With regard suspect to with the usual The require is by genetic bloods. The * Ceppellini,” he either eveists propositus. A single may family affecting each child differemst.ly, excluded. There is no reason to suspect a mutation would seem to be excluded of rare is excluded hel two children, there S 1)0 reason to all other red cell antigens am-c compatille as shown below (cf. table 2). With su(-h un- expectatiOl)s one further possibility the and Furthermore, in two for two propositus theoretical findings nonmatermty one the nonmaternity. the in the same generation, Nondisjunction absence explanation findings however, homozygous of B in the for can systems as the be found that has 11-3, group 11-4, evidence genetic and to the for explanation for of the violatioms in a finer presented heterozygous. blood apparent siblings or an one of indicate possibility since this identical father that amid 111-1, 11-5. heredity the three 8 of the and would twins A1B child, the of of nonpatei’nity. Memidelian analysis 11-6, the adult imi group Oh 9 individuals Le(a+) bloods From www.bloodjournal.org by guest on June 15, 2017. For personal use only. LEVINE ET 1103 AL. I I 00 B? Xx xX ? :ii Se se 5 xx xx ese see :iir I A1B 2 00 Xx xX se In FIG. 2-The the propositus, that the schematic 1)100(1 like Oh are It is possible upon a of the genes factor B and 0 and group nonsecl-etors to explain the both presses Le(a+) Le’ of the the Lewis event, In indeed the above are individual does and in the to are imply not suppressed appears and its kind be linkage. l)hieflOtype 50 a nonsecretor. Le(a+) provide may from anticipated by gene to the later shown be ABO a most. it might recessive of the nature in generation palcI)ts 11-3, 11-4, and The essential The blood India when h)eing made in by Le (a+). Even secretor of ABH the Dr. suppressor on blood exceptional with to Simnsons if Le (a-), substances. full be gemie genetics it is desirable at this to exist recessive tune. between the to be quite definite to its nom-mal In alty suppressor as was allele X l)e- known heterozygotes I-i amid 111-2 of anti-H scm-a. Similarly the B factom and anti-13. If the gene behaved as expression group case to this of the am-c possible to detect selologically the heterozygote tests with anti-H. In further suppom-t of the gene is the histoi-y of consanguinity iii the retest individual of the phenotype of and Simmons in Australia anti_Le suppressiomi status, sup- in I am)d the 11-6. data tested been reactions state bloods Ceppellini.’3 x is assumed have weaker assun)pt.iomi of the secretor seems an knowledge commitlnents locus the presence of a single dose in the could not be detected in tests with a variety in 1-2 behaved normally in tests with anti-H distinctly ABH any cause a dominant, of our by homozygous That all Oh relationship to make the family the in secietion. state relationship independence suppression ABH of genetic not in this x which uncertain am)d relationship its findings gene and of the restraint brilliantly The some view system some Lea, phenotype suggest whatever * given secretion unusual of a rare ABO gene. to exercise by e as of H sul)stance all the interaction would the x and 1)100(1 5e clue.* based to the behaves of phenotype important se arrangement 11-6, 6 o A10 se and a specimen could and saliva which h)e of genes in the genotype, l)’Sena7 is in t lie still the rai’e suppressiomi 7 to days be studied. fresh-b variety 3 homnozygotes state of in geno- transit from Aim attempt is may prove to 1)e Le (a - ) and non- From www.bloodjournal.org by guest on June 15, 2017. For personal use only. 1104 SUPPRESSION type, the results are stlb)stalice Since 11-1, possibly was with given for the contributed is suppressed secretion twins 11-3 there as vet n are Iii red the action of 11-6 derived short, dells gemse transmitted derived i.e., By of the from the mother 11-4, in genotype the Xx, same token, 11-6 as indicated suppressed secretion for the homozygous in 1-2, but The secretor gene by happy coincidence the mentioned group above, also comnpatible fom the Careful members titration folloivimig by other values of the obtained the theoretical of the family sera after and X gene Se i findings in her phenotype also of the be but Sese, of the propositus 1 hour mcubatiomt B in of the Se 111-2 in the secretor he is must father TI-S The reactions of the antigemuc systems inK-k, The in figure genera- omily the the expectations. listed three action secretion are given in table 2. with the Rh-Hr, MN, Ss, Fya, with expression 1 of the the As are the not also cludimig factors genes secretion 6 members and as expected his red cells are Le(a+). of the same 6 imidividuals for the several and the the may xx suppresses mother father I-i. 11-6 because tests its that gene B does not prevent child 111-1 who is by also a nom)secretor red cell antigens blood Let 1. suspected her but in the genotype and Figure this. genes the ABH in 11-6, however, the A1B also whose of scheme and propositus to establish from the from 11-3, is probably of the essential in figure 2. represented secretion B and secretors, it was for B or if heterozygous, gene, 11-5. B to the xx. The suppression, its full penetrance 11-4 progeny inheritance is and and corresponds siblings, ()h father in the The idemitical The the certainly 111-2. tiomis 3 group SUBSTANCE anti_L& in group suppressor by GROUP homozygous by the genotype of gene B and heterozygous plogem)y are is either the to and 1 which 11-7 1-2 transmitted \\.as suppressed the tmansmission being and mother BLOOm) anti_Lea in Table 11-2, the OF 1 and and same table in blood Jka holds true 1. and her two siblings showed the at roomu ternpem-atui-e followed spinmmsg: Test Serum Cells (titer l: __________ ________________________________________ of 0 A2 A, B 16 M. P. 11-3 16 32 64 H. P. 11-4 32 32 64 S I. P. 11-6 32 64 64 32 2 TABLE Secretion No.’ I-i 0 1-2 B A, Oi 11-5 11-6 Lewis Rht MNSs a-b+ DCe/DcE MNSs 0 kk 0 a+b- DCe/DCe + k/c + se a+b- DcE/dce + k/c se a+b- DCe/DCe M Ss M Ss M SS M SS M Ss + + 0 0 k/c kk + k/c A,B se a+b- DCe/DcE 111-2 0 Se a-b+ DCe/dce * The in f Most six individuals Figure for whom 2. probable Jk’ Se se 111-1 those - gemsotype. antigens and ABH secretions are given correspond 0 0 to From www.bloodjournal.org by guest on June 15, 2017. For personal use only. LEVINE The titers were somewhat values of anti-H :256, 1 :256, and 1:32. respomiding as 1 The presence the ii) with of each of the sera of the three med cells and by group specific ET IlOs AL. lower after incubation in the three original three specific for 1 hoimr Bombay antibodies, O, siblings neutralization was at 37 1)loods’ anti-A, C. cor- The weme reported anti-B, amil ammti-H established by specific with secretor salivas absorptiomt amid purified A and B substances of both human* and animal sources. suppressor genotype xx exerts its effect both on the ABH in the red! cells sc(-retion l)ut it has no influence on the agglutinability of the several other tested, M, N, D, and! C. The suppressor gene also did mot affect. the The alid factors reactiomi 11) tests specific antibodies. with rabbit antiserum the suppression With anticipated a compensatory cells amid saliva. Titration that the that found amount Inhibition the whether or miot the t.ions. More of penetrance tive cells propositus of 11-6 An 6 sela, the can be ol)tained 1000 additional cells 5 in group 0 and her prepared sera ram)dlom sera read in group B reacted of the presence of amitiLet. Only omse serum, cells 11-6. This serum was derived from a mother iii group 0 and in 2 in group B. Direct titration salimic amid serum suspended red cells amid B bloods respectively. Apparemit.ly, amid! in the indirect alitiglobulili test imiactive was Of 37 amiti-A of the of gm-oup seruni none of the t.he partially rabbit immune specific In testing react.iomis the the were tested of 11-6 specific X 0 mating for maternal seruns of 1:640 and childremi had neutralized seiies, virtue by with oh- iii ol’dler In this cells was m-ea(-t Nega- B soluble were red to 1 : 512. A sera. with of the seems (legmee failed with group centrifugation. values any was gross 0, he prepama- the med 2 childmemm with both 1:80 fom A, hemolytir matemmial disease serum for A1 amid B bloods. selected group amid anti-B, propositus. anti-Le”. showed 11-4 of all groups in B as complete to to detect after group ramige below. group no same isolated in tests groups, red indhicated showed amid with from of all of agglutimiation one obtained have iii the it remuains of which immunized eluates of 600 11-3 titer species might ) individluals. chensically siblings were in the out in order as described the one Le(a+ siblings but usimsg anti-B, of 11-6 random series degrees and A im)dividuals anti-B weaker cont.aimiing substances however, was substances were carried in the red cells 11-6 red potent with ABH comitaining of 16 group amid (-ells substamice 3 Oh siblings of the experiments B amitigen A sera with substamice to detect. of the result group anti-B served. same of the reactions blood! substances secretion extcmisivc of the pooled amiti-B, red ABH increase in the amount of Lewis and inhibition studies with am)tiLet, of Let of The human of the oms the i-cd cells and in the salivas of normal experiments with the salivas of the three suppression with for Of the B infants, 0 sera 6 gave However, comitaining remaining five three the so-called imumumie to distimiet reactions with ouie of tl)ese could! be attributed weak of group thent 0 suffering sera, four front s’ere hemolytic which am)ti-A the om group to derived the presem-e fromii disease. 1)0th O, bloods of mriothers The fifth reacted! with the blood of the propositus was derived from a male imidividlual who received! imijeetiomis of A and B specific soluble substamices. Theme is iio imidlicatiomt that the degree of reactivity with red cells ran parallel to the dhre(-t titer of anti-B nor to the titer of the so-called! immuumie anti-B in tests of the Oh * Supplied by l)r. Elvin A. Kabat. From www.bloodjournal.org by guest on June 15, 2017. For personal use only. 1106 SUPPRESSION partially tiOli neutralized Eluates the of for semum. BLOOD This GROUP aspect SUBSTANCE of the B subject merits further light of the findings with eluates. front the red cells of the three siblings after group 0 sera (anti-B 1 : 2048) gave reactions invest.iga- in the especially one OF prepared active the exposure to a titer of to 1:4 B hut also two other from B cell 1 : 2 for A1. (Similar results were obtained with eluates prepared active group 0 sera.) With the same serum eluates front a normal titers of 1 : 256 and 1 : 2 for B and A1 bloods respectively. This suggests gave that it is the cross-reactive antibody in group for the greatly suppressed B factor not yet comuplete and further studies of a group lyt.ic A mother whose group in the are 0 sera’4 which Oh bloods. The required especially B (or group AB) has weak affinity evidence, however, is with the rare serumu infant is affected with hemo- disease. That the in part, effect may 11-6, positus, tered With almost of penetrance affinity a failure after to exposure which anti-A he attributable by indicated in the group 0 serum with the blood active hemolytic is, at least of the pro- eluates 0 serum to a group caused complete to anti-B obtain containing an equally high-ti- disease. suppression of the B antigems, the only manifestation is some residual antigenic component which apparently the cross-reacting antibody in selected group 0 sera. for has an DIsCussIoN The plified interpretation by having superficial of the findings in available all members inspection of the factor andi secretion two children. It is greatly to phenotype three Lewis nismn Bolnhay and ABH might, the credit bloods, under data this remarkable family of the three generations figure in in the 1 suggest.ed propositus of CeppellinP3 anticipated who, the secretion systems. special conditions, He the ozygous genes offspring. The aie tral)smitted on analyzing of the expression the further to include data their also red cell the antigens 0 and/or although the respective family presented in this effects fully expressed B in her imi the of gene interaction speculated that the same be extended and suppression full possibility Ceppellini13 states that “in these three individuals B do not manifest themselves on the red cells, present in the genotype”, and, as shown in the cation, the amid their group was sunso that even a of the mechaantigens. A and/or genes are commumsi- in the heter- * findings in this family do not adversely influence the usefuimsess of blood of disputed paternity because the Oh type of blood with suppressed he readily detected by the presence of anti-H in the serum. Assuming the in cases tests B can operatioms of the same mechanism in the 9 other ported in the literature, the specific blood factor only by complete family studies. It appears that India. Blood! group amstigens human heredity because frequently fully * of Oh with anti-H could be determined gene occurs re- more 111 expressed The examples suppressed the suppressor above have been considered the products of the in all instances. quotation is In short, Ceppellini’s the translation to be luost genes involved degree from useful in the study of were believed to he of penetrance his Italian was book.’3 consideredi From www.bloodjournal.org by guest on June 15, 2017. For personal use only. LEVINE to be imivariahly complete. The group constitutes an exception to this that a similar mechanism may other blood group systems. A family is of the family be explained of cases Se ozygous reveals tree AND in which the anti-H in addition apparent same 0 blood!s com)t.ainil)g commumsication findings, serologic it is possible findings un del e anti-B. Le del and to anti-A 2 siblings, apparently and Inspection anti-B. of Mendelian heredity which can state genes heter- gene. he assumed familia to operate examim)e the in 9 other so-called group del arbore seros e duo pote de anticorpores genealogic que in le stato INTERLINGUA le proposita 0, ha in br mendelian ue IN que in gruppo hereditate gets suppressor in anti-H. pmesemstate parem)temente tiol)es propositus violations SUMMARIO Es in this of these unusual CONCLUSIONS sera the suppression mechanism may for The their 11) discussed oms the basis of a rare suppressor gene which in the homozygote us the propositus the actions of gene B and secretion gene Se. The are fully expressed when transmitted to her offspring who are suppresses B and presented 0, have 1107 AL. rule. In the light serve to explain SUMMARY in gi-oup ET del esser homozygotic su consanguineos, anti-H familia revela apparente explicate super le base supprime ap- in ultra in le proposita de anti-A violade un rar le action del geis B e dcl gen de secretion Se. Le genes B e Se es completemente exprimite quando illos es transmittite al prole del proposita, proque le prole es heterozygotic pro le gems suppressor. On le mesme de sanguines supponer que ims Ic litteratura, pote reportate mechanismo del es gruppo active le in 9 altere 0 continente casos, anti-H. ADDENDUM After this tentiomi to manuscript was a strikingly parallel the alleles for t.he secretion types r sire xi (Ian) yielded resented as r/r sile xR/r ii amid this Irwin, M. in sheep. factors, offspring dam and Professor M. of suppressor R., R/r offspring, but the suppresses the offspring. (Rendel, Evidence for epistatic 396-408, 1954.) Genetics II. Irwin called our atgene called i involving R and r in sheep. Thus, of type R. Genotypically, homozygous state presumnably appears in the heterozygote however, and submitted, example action of genes a mating the dam R/r of phemio- mating is rep- is of genotype expression of R which, J., Sorensen, A. N., for antigermic substances 39: REFERENCES Y. M., ‘BHENDE, W. T. J., R.: GRUBB, Some et Microb. Boyn, WATKINS, Lamicet system. 2 AND W. secretors 1195-1198, 1: 903-906, aspects Scand. C., C. K., W. M.: DESHPANDE, AND and 1954. H. M., II., RACE, II. H., SANGER, blood-group “new” character related to MORGAN, the ABO 1952. of the Supp. con)l)lexity of the human ABO blood groups. Acta Path. 84, 1949. E.: SHAPLEIC;mr, nonsecretors I3HATIA, A by Separation use of a of l)laflt individuals agglutinin of (Lect.in). any blood group Blood 9: No. into 12, From www.bloodjournal.org by guest on June 15, 2017. For personal use only. 1108 SUPPRESSION L., HIRSZFELD, OF R.: AMZEL, AND des pleiades. Ann. Inst. W. T. J., AND MORGAN, J. Exper. Path. KOTHARE, B. V., BHATIA, Brit. 6 case. SUBSTANCE pleiades B “isoseriques” 386-414, W. M.: of the du sang. Sur l’heredite 1940. The so-called detectioim 0 of a product substance to the of the blood agglutinogens group A and B. 1948. 159-173, H. M., SUKUMARAN, P. K., BHATIA, PARKIN, SANGHVI, AND L. I).: Unpublished H. M., SANGHvI, Paper DOROTHY: Paris, R.: presence September, anti-O of of human blood R.: m2 CEPPELLINI, International NASSO, I.S.M.S.B., specimens, L. D., presented 0 blood. J. Indian M. A. JHALLA, H. I.: In preparation, 1955. Congress of Blood Tranis- 24: No. AND MORGAN, and secretions. On the S., at the the secretioii in serum. human W. T. J.: genetics 1952), p. 204. R. E.: A-B hemolytic with special reference Blood 10: No. Vox International 1, 17-28, “La and observations 78, group amitigens the and 1952. on the 1-2, 1-14, 1955. Lewis characters: Paris, malattia disease to the 1955. 170: 0 amid H characters 5, No. Transfusion. F.: of the blood Nature Some Sang. of secretor of Blood TEzILAcIcH, AND Y. G., Fifth between or anti-H Congress BHIDE, 1954. A relationship W. M., “WATKINS, “ROSENFIELD, in group 1955. fusions. ‘#{176} SANGER, G. W. L.: Anti-H R. T., AND D’SENA, 9, 325-327, mother. les 65: WATKINS, 9: GROUP 1953. SIMMONS, 13_, Sur Pasteur. and the relationship O gene BLOOD A faniily 1954. September, emolitica of the newborn. direct antiglohulin del study. (Milan: neonato” Analysis of test and Fifth 1480 to cord the Ed. 1)lood group 0 From www.bloodjournal.org by guest on June 15, 2017. For personal use only. 1955 10: 1100-1108 Gene Interaction Resulting in Suppression of Blood Group Substance B PHILIP LEVINE, ELIZABETH ROBINSON, MARINO CELANO, OLIVE BRIGGS and LEROY FALKINBURG Updated information and services can be found at: http://www.bloodjournal.org/content/10/11/1100.full.html Articles on similar topics can be found in the following Blood collections Information about reproducing this article in parts or in its entirety may be found online at: http://www.bloodjournal.org/site/misc/rights.xhtml#repub_requests Information about ordering reprints may be found online at: http://www.bloodjournal.org/site/misc/rights.xhtml#reprints Information about subscriptions and ASH membership may be found online at: http://www.bloodjournal.org/site/subscriptions/index.xhtml Blood (print ISSN 0006-4971, online ISSN 1528-0020), is published weekly by the American Society of Hematology, 2021 L St, NW, Suite 900, Washington DC 20036. 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