• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
13_DetailLectOut_AR
13_DetailLectOut_AR

... The number of combinations possible when chromosomes assort independently into gametes is 2n, where n is the haploid number of the organism.  If n = 3, there are 23 = 8 possible combinations.  For humans with n = 23, there are 223, or more than 8 million possible combinations of chromosomes. ...
Modern Genetics PPT
Modern Genetics PPT

... Genes carried on the sex chromosomes  A female has 2 X chromosomes: if one x has a dominant gene and the other has a recessive, the dominant trait will show  In a male, there isn't corresponding alleles. If the X chromosome has a recessive trait, and there is no corresponding allele on the Y chrom ...
No Slide Title
No Slide Title

... XXX Condition (Poly X females) • The presence of three X chromosomes along with a normal set of autosomes (47,XXX) results in female differentiation • Frequently, 47,XXX women have no distinctive features other than a tendency to be tall and thin. • 1 in 1000 female births • Although a few are ster ...
Extracting and Isolating Your Own DNA
Extracting and Isolating Your Own DNA

... groups of _________________ proteins, like ______________ on a string. This complex of DNA and proteins is called _________________________, and when it coils around on itself it forms neat packages called chromosomes. Page 2 of 4 ...
2.1 Mitosis + Meiosis notes
2.1 Mitosis + Meiosis notes

... normal number of chromosomes than the regular body cells (autosomes). When the sperm and egg unite the resulting zygote will contain the normal number of chromosomes for that organism. A special process called meiosis occurs in the reproductive organs to allow this to occur. Meiosis is a bit more co ...
Nature of Sex Chromosomes
Nature of Sex Chromosomes

... usually remains unchanged from generation to generation but changes do sometimes occur and the number of repeats may increase or decrease. ...
Shared character
Shared character

... When the chromosomes are stained, showing pattern of bands, and those band have same pattern in same region of similar chromosomes, the regions are likely to have been inherited from 1 chrom. In last common ancestor of 2 species o When chromosomes have similar banding patterns, they may be homologou ...
Mendelian Genetics
Mendelian Genetics

... • In fruit flies and humans traits carried on the X chromosome are said to be sex-linked. • A recessive gene on the X chromosome will always be expressed in the male, since there is a single X present. • A female with the recessive gene on one of her two X chromosomes will be able to pass the trait ...
Evolution (cont.) - leavingcertbiology.net
Evolution (cont.) - leavingcertbiology.net

... 2. Those organisms with the most beneficial variations (adaptations) will survive and pass on those characteristics to their offspring ...
CYTOGENETIC STUDIES OF PRECOCIOUS MEIOTIC
CYTOGENETIC STUDIES OF PRECOCIOUS MEIOTIC

... proportion of cells at MI having only bivalents. All the centromeres divided precociously during this stage in these cells, although sister chromatids did not fall apart until homologues had migrated to opposite poles at AI. Each daughter nucleus thus contained the unreduced chromosome number. The s ...
Meiosis and Fertilization
Meiosis and Fertilization

... A human embryo with that many chromosomes in each cell would be abnormal and would die before it could develop into a baby. So, gametes can not be made by mitosis. 3. Each human sperm and egg should have ____ chromosomes, so fertilization will produce a zygote with ____ chromosomes; this zygote will ...
Ch 13 outline
Ch 13 outline

... The number of combinations possible when chromosomes assort independently into gametes is 2n, where n is the haploid number of the organism.  If n = 3, there are 23 = 8 possible combinations.  For humans with n = 23, there are 223, or more than 8 million possible combinations of chromosomes. ...
Study guide for Chapter3: Cell division and Chapter 4
Study guide for Chapter3: Cell division and Chapter 4

... Please use the following resources as you complete this study guide: Ttextbook pages C 73-92, C117-119 and C 135-136 1. Define the following terms: Chromosomes, Chromatids, DNA, Cell cycle, Haploid, Diploid Cell Division, Unicellular, Multicellular, Prokaryotic, Eukaryotic, Nucleus, Fertilization, A ...
I Gregor Mendel - Nutley Public Schools
I Gregor Mendel - Nutley Public Schools

... a. ________________: monosomy where the individual has single X chromosome. b. ________________is most common trisomy among humans; it involves chromosome 21. 6. Polyploidy: offspring end up with more than two complete sets of chromosomes. a. Terms indicate how many sets of chromosomes are present ( ...
High Mutation Rates Have Driven Extensive Structural
High Mutation Rates Have Driven Extensive Structural

... Gene conversion acts at a slow rate. Balanced between rates of mutations that cause differences between arms. Indicates that process may not be driven by selective constraints, but rather a weak direction bias which favours preservation of original sequences.(at least in humans) ...


... The above two classes of proteins combine to form a ...
Mid-Term Exam 3a - Buffalo State College Faculty and Staff Web
Mid-Term Exam 3a - Buffalo State College Faculty and Staff Web

... 1. Print your name in the space designated on this cover sheet. 2. Be sure that your exam has 9 pages including this cover sheet. 3. Read each question carefully and answer in the space provide 4. At the end of the exam there are 6 short answer questions. Answer only 5 of these 6 questions. Answerin ...
Based on the study of probability
Based on the study of probability

... • Both alleles of a gene express themselves= both proteins are produced • Examples: – AB blood type (protein “A” and protein “B”) – Sickle cell trait ( point mutation in hemoglobin)produces 3 phenotypes- normal, trait, anemia ...
Topic 2 & 3: Genetics Review
Topic 2 & 3: Genetics Review

... • Shaded symbols indicate individuals showing the trait • Horizontal line connecting male and female signifies reproduction (or marriage) • Offspring are listed below in birth order ...
Genetics - Mother Baby University
Genetics - Mother Baby University

... chromatin to be incorporated into one of the daughter nuclei following cell division as a result of delayed movement during anaphase ...
X w
X w

... Heterogametic sex- Producing gametes that contain two types of chromosomes (males in mammals and insects, females in birds and reptiles) ...
Mitosis/Meiosis and Genetic Diseases
Mitosis/Meiosis and Genetic Diseases

... -Deletion – removal of a chromosomal segment (as seen in 22q11.2 deletions in Velo-Facial-Cardiac Syndrome) -Inversion – reversal of a segment within a chromosome This can cause altered gene activity, a loss of crossingover, or a duplication/deletion if crossing-over does occur. -Duplication – repe ...
Biology - Saunders' Science
Biology - Saunders' Science

... This chromosome forms a dense region in the nucleus known as a Barr body. Barr bodies are generally not found in males because their single X chromosome is still active. Slide 12 of 25 Copyright Pearson Prentice Hall ...
Exam Study Guide
Exam Study Guide

... 84. How many recessive alleles are necessary to see a recessive trait? 85. Rate each of the following as passive or active transport: osmosis, diffusion, facilitated diffusion, molecules moving from lesser concentration to greater concentration **You will be given different scenarios and will have t ...
Genetics
Genetics

... ...
< 1 ... 257 258 259 260 261 262 263 264 265 ... 435 >

Karyotype



A karyotype (from Greek κάρυον karyon, ""kernel"", ""seed"", or ""nucleus"", and τύπος typos, ""general form"") is the number and appearance of chromosomes in the nucleus of a eukaryotic cell. The term is also used for the complete set of chromosomes in a species, or an individual organism.Karyotypes describe the chromosome count of an organism, and what these chromosomes look like under a light microscope. Attention is paid to their length, the position of the centromeres, banding pattern, any differences between the sex chromosomes, and any other physical characteristics. The preparation and study of karyotypes is part of cytogenetics. The study of whole sets of chromosomes is sometimes known as karyology. The chromosomes are depicted (by rearranging a photomicrograph) in a standard format known as a karyogram or idiogram: in pairs, ordered by size and position of centromere for chromosomes of the same size.The basic number of chromosomes in the somatic cells of an individual or a species is called the somatic number and is designated 2n. Thus, in humans 2n = 46. In the germ-line (the sex cells) the chromosome number is n (humans: n = 23).p28So, in normal diploid organisms, autosomal chromosomes are present in two copies. There may, or may not, be sex chromosomes. Polyploid cells have multiple copies of chromosomes and haploid cells have single copies.The study of karyotypes is important for cell biology and genetics, and the results may be used in evolutionary biology (karyosystematics) and medicine. Karyotypes can be used for many purposes; such as to study chromosomal aberrations, cellular function, taxonomic relationships, and to gather information about past evolutionary events.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report