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A Retrospective Study of Balanced Chromosomal Translocations in
A Retrospective Study of Balanced Chromosomal Translocations in

... KEYWORDS Balanced Translocation. Karyotyping. Phenotypic Features. Chromosomal Rearrangements. Cytogenetic Analyses. Recurrent Miscarriage ABSTRACT The balanced translocations are accepted as chromosomal rearrangements that do not generally reflect any phenotypic evidence. However, phenotypical infl ...
Population Structures of the Red Fox
Population Structures of the Red Fox

... structures on the island could also help to understand some ecological phenomena of the red fox in Hokkaido. For example, sarcoptic mange, which is a serious skin disease of red foxes caused by the mite (Sarcoptes scabiei) and spread by physical contact, has expanded from eastern to western Hokkaido ...
Two novel heterozygous mutations of EVC2 cause a mild phenotype
Two novel heterozygous mutations of EVC2 cause a mild phenotype

... which all coding exons of both genes were sequenced [Tompson et al., 2007]. With the exception of two families reported by Temtamy et al. [2008], all EvC patients screened so far have been shown to have mutations in either EVC or EVC2, when mutations could be found, and so the patient in our study, ...
pdf file
pdf file

... show that the observed patterns of continuous variation were entirely consistent with Mendelian inheritance. He was also able to consider the effects on these traits of various other modifying factors like dominance, linkage and non-random mating. Moreover, he developed techniques for partitioning t ...
CROSSING-OVER IN DROSOPHILA is closer to a spindle fibre
CROSSING-OVER IN DROSOPHILA is closer to a spindle fibre

... the two sections of chromosome III and the homologous unbroken third chromosome are attracted together. These counter-forces working on the broken third chromosome would be expected to interfere with synapsis and presumably also with crossing-over. This explanation obviously cannot be applied to the ...
Felix I D Konotey-Ahulu FGA Key Achievements: National and
Felix I D Konotey-Ahulu FGA Key Achievements: National and

... and ACHEACHE (3 of us) who suffered hereditary cold-season rheumatism, or Sickle Cell Disease. Only the ACHEACHE have symptoms. The kanad enables anyone who knows his/her phenotype to find out which phenotypic pairing will guarantee a non ACHEACHE offspring [Publications 44, 225, 236, 243, 254]. One ...
Review Questions for Respiration
Review Questions for Respiration

... Review Questions for Mendelian Genetics ...
投影片 1
投影片 1

... when he began to experiment with trait inheritance in plants in 1892. Correns already knew about some of Mendel's hawkweed plant experiments from Nägeli. Nägeli, however, never talked about Mendel's key pea plant results, so Correns was initially unaware of Mendel's laws of heredity. ...


... However, several significant interactions with asthma at 6 years of age were found (fig. 1). In the stratified analysis, children with the AA genotype of TLR4 rs2737190 were found to have an increased risk of developing asthma when colonised with H. parainfluenzae at preschool age (OR 0.25 (95% CI 0 ...
Association of estrogen receptor β gene polymorphisms with bulimic
Association of estrogen receptor β gene polymorphisms with bulimic

... This study shows an association between disease and the 1730 G-A and ERb cx þ 56 G-A ERb gene variants for this group of bulimic women. Identification of novel variants of the ERb gene The association described above could exist either because changes at the nucleotide positions in question affect E ...
introduction to genetic epidemiology
introduction to genetic epidemiology

...  The heuristic interpretation is that aggregation exists when cases of disease appear in families more often than one would expect if diseased cases were spread uniformly and randomly over individuals: “it runs in the family”  Actual approaches for detecting aggregation depend on the nature of the ...
video slide - Point Pleasant Beach School District
video slide - Point Pleasant Beach School District

... example, used by various cells, or has a signaling function on various targets. ...
19. - 21. März 2014 in Essen - Deutsche Gesellschaft für
19. - 21. März 2014 in Essen - Deutsche Gesellschaft für

Genetic structure of captive and free
Genetic structure of captive and free

... to be due to the fact that, for some species, mtDNA has been shown to feature low diversity in the wild and/or founding individuals, limiting its utility (Hedrick et al. 1997). However, due to the unique inheritance of mtDNA (haploid, non-recombining and maternally inherited), it can also provide in ...
Incipient allochronic speciation due to non
Incipient allochronic speciation due to non

... Mutation occurs during meiosis independently for alleles at each locus with probability mZ U =ð2nÞ per generation, where U is the genomic mutation rate for flowering time. The mutational variance is s2m Z U s2m , such that changes in allelic effects of new mutations are normally distributed with mea ...
Epidemiologic and Genetic Approaches in the
Epidemiologic and Genetic Approaches in the

... When one of the factors is rare in a geneenvironment interaction study, the two-stage or multistage design may be appropriate. These designs increase the numbers of cases and controls with the rare factor without prohibitively increasing the number of measurements to perform. For two-stage study des ...
20656341304a5aa0f70818a
20656341304a5aa0f70818a

... Fig. 2-2.: The iodide cycle. Ingested iodide is trapped in the thyroid, oxidized, and bound to tyrosine to form iodotyrosines in thyroglobulin (TG); coupling of iodotyrosyl residues forms T4 and T3. Hormone secreted by the gland is transported in serum. Some T4 is deiodinated to T3. The hormone exe ...
Dr Noor Lita Adam 260609
Dr Noor Lita Adam 260609

... Fig. 2-2.: The iodide cycle. Ingested iodide is trapped in the thyroid, oxidized, and bound to tyrosine to form iodotyrosines in thyroglobulin (TG); coupling of iodotyrosyl residues forms T4 and T3. Hormone secreted by the gland is transported in serum. Some T4 is deiodinated to T3. The hormone exe ...
Evolutionary adaptation to high altitude: A view from
Evolutionary adaptation to high altitude: A view from

... growth studies conducted by Frisancho and Baker (1970) showed, through comparisons of age groups, a delayed adolescent growth spurt in high-altitude adolescents, illustrating another important example of the usage of time. Whether by cross-sectional comparison of different age groups or, better yet, ...
The Jumping SHOX Gene—Crossover in the Pseudoautosomal
The Jumping SHOX Gene—Crossover in the Pseudoautosomal

... percentage could be due to the fact that males with LWD are overrepresented in the families. The possibility of a crossing over seems not to be dependent on the kind of abnormality in PAR1. Flanagan et al. (16) described one family with at least a deletion of the whole SHOX gene and one family with ...
Name: Period - WordPress.com
Name: Period - WordPress.com

... Background: In this activity, you will examine natural selection in a small population of wild rabbits. On a genetic level, evolution is a change in the frequency of alleles in a population over a period of time. Breeders of rabbits have long been familiar with a variety of genetic traits that affec ...
Document
Document

... property called pleiotropy • Pleiotropic alleles are responsible for the multiple symptoms of certain hereditary diseases, such as cystic fibrosis and sickle-cell disease ...
MQ (54) LIV 2 contents
MQ (54) LIV 2 contents

... all ten SNPs was performed with oblimin rotation, to test the prediction derived from the polygenic selection model, that a positive statistical correlation between frequencies of alleles associated with the same trait should be observed. PCA was chosen on the basis that as molecular measures, the r ...
The long-term evolution of multi- locus traits under
The long-term evolution of multi- locus traits under

... Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum. ...
julian huxley: developmental genetics and the theory of evolution
julian huxley: developmental genetics and the theory of evolution

... speeds. He observed that the speeds were average in heterozygote hybrids with intermediary coloring. At the beginning period of his scientific career, he was an embryologist and united embryological and genetic explanations. The narrow differences between adult forms, for him, can be the result of w ...
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Medical genetics

Medical genetics is the specialty of medicine that involves the diagnosis and management of hereditary disorders. Medical genetics differs from human genetics in that human genetics is a field of scientific research that may or may not apply to medicine, but medical genetics refers to the application of genetics to medical care. For example, research on the causes and inheritance of genetic disorders would be considered within both human genetics and medical genetics, while the diagnosis, management, and counseling of individuals with genetic disorders would be considered part of medical genetics.In contrast, the study of typically non-medical phenotypes such as the genetics of eye color would be considered part of human genetics, but not necessarily relevant to medical genetics (except in situations such as albinism). Genetic medicine is a newer term for medical genetics and incorporates areas such as gene therapy, personalized medicine, and the rapidly emerging new medical specialty, predictive medicine.
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