1.poly-x syndrome
2.turner syndrome
3.klinefelter syndrome
4.jacob syndrome
Observation: Sex Chromosome Anomalies A female with Turner syndrome (XO) has only one sex chromosome, an...
Aneuploidy of an autosome is always more harmful than an aneuploidy of a sex chromosome. One of the explanations as to why sex-chromosome aneuploids are less harmful is due to X inactivation. X-inactivation assures that all human cells only express a single X chromosome regardless of how many X chromosomes are present. Interestingly, sex chromosome aneuploids (i.e. XXY, XO) still have some different phenotypes compared to either an XX or XY individual. For instance, XXY individuals (Klinefelter Syndrome) are taller, have...
22. [9 PTS] Turner syndrome results when an individual has a genotype of XO (a single X chromosome), and no other sex chromosomes. Color-blindness results from mutation of a single gene on the X chromosome. A couple, both of whom have normal color vision, have a color-blind child with Turner's syndrome. a. Did non-disjunction occur in the mother, or the father, or is it impossible to tell? Explain your answer. (3 pts) (continued next page. b. In the space provided...
Genetics question!! Please help with these 3. Thanks A woman with Turner syndrome (X0-only one X-chromosome) is also colorblind (an X-linked recessive phenotype). Both of her parents have normal color vision. This women's karyotype and genotype could have arisen by: a) a mutation in her mother's X-chromosome b) non-disjunction in mitosis c) non-disjunction in meiosis 1 in her father d) non-disjunction in meiosis 2 in her mother e) non-disjunction in meiosis 1 in her mother 10. Mitochondrial genomes a) replicate...
A human zygote (a fertilized human egg) has an abnormal sex chromosome genotype of XO meaning that the zygote only has a single X chromatid and no other sex chromosomes. This abnormal genotype could have resulted from (note: to earn full credit you must correctly select ALL that are possible for resulting in an XO zygote). -a single nondisjunction event in meiosis I in the female parent -a single nondisjunction event in meiosis II in the female parent -a single...
1.a) How do we know that in humans the X chromosomes play no role in sex determination, while the Y chromosome causes maleness and its absence causes femaleness? c) How do we know that X chromosomal inactivation of either the paternal or maternal homolog is a random event during early development in mammalian females? d) How do we know that Drosophila utilizes a different sex-determination mechanism than mammals, even though it has the same sex-chromosome compositions in males and females?...
Question 1 1 pts Sex determination in mammals is due to the SRY region of the Y chromosome. An abnormality of this region could allow which of the following to have a male phenotype? O a person with an extra X chromosome Turner syndrome, 45, X O Down syndrome, 46, XX O a person with one normal and one shortened (deleted) X O translocation of SRY to an autosome of a 46, XX individual Question 2 1 pts What does...
D) A and B only E) A, B, and C 25. Which of the following statements are TRUE? A) It is possible for some individuals with the sex chromosome constitution XY to appear female. B) It is possible for some individuals with the sex chromosome constitution XX to appear male. C) It is possible for some individuals with the sex chromosome constitution XXY to appear female. D) All of the above are FALSE statements. E) All of the above are...
19) Trisomy 21, or Down syndrome, occurs when there is a nom complement but one (extra) chromosome 21. Although fertility is reduced in both sexes, females have higher fertility rates than males. Van Dyke et al. (1995; Down Syndrome Research and Practice 3(2):65-69) summarize data involving children born of Down syndrome individuals. Assume that children are born to a female with Down syndrome and a normal 46-chromosome male. What proportion of the offspring would be expected to have Down syndrome?...
Solve It: Does Sex Determination Have Only Two Possible Outcomes: Male or Female? One of the most fundamental aspects of personhood is your biological sex: "It's a girl" or "It's a boyl" is often the first statement about who you are. Most people view biological sex as a straightforward, eitherfor issue-either a person is biologically male or biologically female. Like all biological characteristics, however, sex determination is achieved through a developmental process. All developmental processes exhibit variation, and sex determination...
Merfolk have three pairs of autosomes and one sex chromosome; males are XO and females are XX. In merfolk the genes controlling tail fin shape and scale colour are on different autosomes. Solid tail fin (Ff) is dominant to forked tail fin (ff), and the Fallele is recessive lethal. There are two alleles of the scale colour gene - CB(blue) and CR (red)- CB and CR show incomplete dominance with heterozygotes being purple. The silent trait is X-linked and dominant...