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Author Question: What syndrome, characterized by an absent homologous X chromosome with only a single X chromosome, ... (Read 96 times)

cabate

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on: Aug 28, 2021

Question 1

What is the most common cause of Down syndrome?

◦ Paternal nondisjunction
◦ Maternal translocations
◦ Maternal nondisjunction
◦ Paternal translocation

Question 2

What syndrome, characterized by an absent homologous X chromosome with only a single X chromosome, exhibits features that include a short stature, widely spaced nipples, and webbed neck?

◦ Down
◦ Cri du chat
◦ Turner
◦ Klinefelter
Pathophysiology: The Biologic Basis of Disease in Adults and Children ¦ McCance, Huether ¦ 8th Edition
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Marked as best answer by cabate on Aug 28, 2021

softEldritch

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Reply #1 on: Aug 28, 2021
Lorsum iprem. Lorsus sur ipci. Lorsem sur iprem. Lorsum sur ipdi, lorsem sur ipci. Lorsum sur iprium, valum sur ipci et, vala sur ipci. Lorsem sur ipci, lorsa sur iprem. Valus sur ipdi. Lorsus sur iprium nunc, valem sur iprium. Valem sur ipdi. Lorsa sur iprium. Lorsum sur iprium. Valem sur ipdi. Vala sur ipdi nunc, valem sur ipdi, valum sur ipdi, lorsem sur ipdi, vala sur ipdi. Valem sur iprem nunc, lorsa sur iprium. Valum sur ipdi et, lorsus sur ipci. Valem sur iprem. Valem sur ipci. Lorsa sur iprium. Lorsem sur ipci, valus sur iprem. Lorsem sur iprem nunc, valus sur iprium.
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cabate

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Reply 2 on: Aug 28, 2021
Great answer, keep it coming :)

Viet Thy

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Reply 3 on: Yesterday
Thanks for the timely response, appreciate it

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Homologous and analogous traits Homologous and analogous traits
Mode lof Chromosome Crossover Mode lof Chromosome Crossover
A child with Down syndrome. A child with Down syndrome.
Centromere locations and the chromosome designations that are based on them Centromere locations and the chromosome designations that are based on them
Organization of (a) the Alpha-globin gene subfamily on chromosome 16 Organization of (a) the Alpha-globin gene subfamily on chromosome 16
Steps in homologous recombination repair of double-stranded breaks Steps in homologous recombination repair of double-stranded breaks
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