Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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Trisomy 21, or Down syndrome, occurs when there is a normal diploid chromosomal complement but one (extra) chromosome 21. Given the fact that embryos with 48 chromosomes (four #21 chromosomes) are not likely to survive early development, what percentage of surviving offspring would be expected to have Down syndrome if both parents have Down syndrome?
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- Which of the following conditions is not the result of a chromosomal alteration? ○ Chronic myelogenous leukemia (CML) ◇ Down syndrome (Trisomy 21) Turner syndrome O Mosaicismarrow_forwardNondisjunction which can affect sex chromosomes as well as autosomal chromosomes as a common cause of genetic disorders. Use the space provided to illustrate the process of nondisjunction with the end result being that one cell exhibits in the monopsony me while other one exhibits trisomy. Hint: a sperm will fertilize the egg and add it’s chromosome in the last step)arrow_forwardAbnormal chromosome division during mitosis can result in 47,XXX syndrome. Which statement regarding 47,XXX syndrome is FALSE? -Those with 47,XXX syndrome have 3 copies of chromosome 47 -Thise with 47,XXX may have interllectual disabilities -47,XXX syndrome occurs only in the female sex -47,XXX results in a mosaic phenotypearrow_forward
- In fruit flies, chromosomal crossing over does not occur in meiosis in males, whereas crossing over does occur in meiosis in females. In fruit flies that are heterozygous at many genes (i.e. many maternal and paternal versions of the genes differ), at what stage would cells no longer be heterozygous for any gene during the process of meiosis? a)After the second meiotic division in males, and after the first meiotic division in females. b)After the second meiotic division in both males and females. c)After the first meiotic division in both males and females. d)After the first meiotic division in males, and after the second meiotic division in females.arrow_forwardIdentify each of the following statements as true or false. The chromosomes in B are the result of mitosis from the chromosomes in A. Alleles B and C are more likely to segregate together during anaphase I than alleles B and A. The two white chromosomes in B are homologous chromosomes. Genes A, B, and C are linked genes. A trihybrid Punnett square can be used to determine the possible combinations of the F1 generation.arrow_forwardKnowing that wrong number of chromosomes has serious, usually lethal consequences, briefly describe the most common inherited abnormalities in case of trisomy 21 and trisomy 13.arrow_forward
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