The following pedigree represents the inheritance of a rare
disorder in a large
family What is the most likely mode of inheritance? Why?
The following pedigree represents the inheritance of a rare disorder in a large family What is...
Each of the following pedigrees shows the inheritance of a rare genetic disorder. What is the most likely mode of inheritance for each disorder? Explain your reasoning.
A rare human disease is found in a family as shown in the accompanying pedigree. a) Deduce the most likely mode of inheritance b) What would be the outcomes of the following mattings between cousin 3X9? 21. TOD 1 1 2 3 4 5 6 7 8 9 10 TT I Arial 5 (18pt] TEE 25 Path: P Words:0
Question 20 This pedigree (Pedigree #1) illustrates the inheritance of a simple Mendelian disorder. What is the likely mode of inheritance A autosomal dominant B. autosomal recessive C. cannot be determined from the information given D. (This is not a choice.) A Moving to another question will save this response.
1. Human inheritance patterns (5 pts). All of the following questions refer to the following pedigree, tracing a rare trait (#1) and a common trait (#2) through the same family. (We are combining two different charts into one chart with this method. It may help you to redraw two separate charts to make who is affected/unaffected by each trait more clear. The inheritance of trait 1 doesn't influence the inheritance of trait 2.) 1 - Affected Trait 1 - Affected...
This pedigree (Pedigree #1) illustrates the inheritance of a simple Mendelian disorder. What is the genotype of individual II-2? OAA B. MA OC. Aa D.aa
The pedigree below shows the inheritance of a rare mutant phenotype in humans, congenital cataracts. If we use the letter E to represent the alleles for this disorder, what are the possible genotypes for person A? ーーーーー -O C Y e YYX Ee eE A EEeXXX NOOOO B
93. The pedigree below shows the sex-linked recessive inheritance of Nance-Horan syndrome, a rare Mendelian disorder in which affected persons have cataracts and abnormally shaped teeth. What is the probability that the first child of IV-6 and V-3 would have Nance-Horan syndrome? Iv A) 114 B) 1/2 C) 1/8 D) 3/16 E) 3/4
3. (10pts) The following pedigree represents a family with a very rare inherited trait in which several haplotypes of an LD block (1,2,3,4) are also segregating. Ι 22 13 3 23 34 11 OOLOOLOOI OOOOOL 24 34 13 24 12 34 12 12 34 14 13 14 14 13 13 13 a. Are the trait and the LD block linked? Your answer should include an explanation of the reasons why you think they are or are not linked. b. What...
answer all plz:) 4. Identify the mode of inheritance for each pedigree. (6 pts) O O 마 0 0 - 5. This pedigree shows a family with a rare condition. (8 pts) a. What is the mode of inheritance of this condition? b. What is the probability that the unborn child at the bottom will display the condition? 명이 1 1 2 5 6 7 8 9
ww Dong 7. This family has members who suffer from a rare disorder (abbreviated PMĚ) that presents with action myoclonus, and progressive neurological decline. (6 pts) Figure 1. Family pedigree and magnetic resonance imaging. (A) The six-generation family showing segregation of PME and ataxia. (B) Normal brain MRI of proband at 9 years. (C) Brain MRI of younger affected sister at 18 months showing callosal agenesis, a large interhemispheric cyst and simplified gyration frontally. PME a. What is the mode...