The modes of pedigree are:-
4-(a):-autosomal recessive
(b):-autosomal dominant
5-(a):-autosomal recessive
answer all plz:) 4. Identify the mode of inheritance for each pedigree. (6 pts) O O...
The mode of inheritance for the following pedigree is X-linked recessive. - O 1 2 3 4 5 6 N III O 1 2 3 5 6 IV 1 2 If individuals III-1 and III-2 were to have another child, what is the probability that they would express the trait? Explain your reasoning.
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) B. (b) In pedigree B, circle all individuals who are heterozygous. (2 pts) OG 0 0 0 0 0 호 c GO GO CD p. | 8 日 ITE | ODDC D Choices: A. Y-linked, B. X-linked dominant C. recessive, D. Autosomal dominant, E. Autosomal recessive.
Part B - Identify the mode of inheritance Look over the pedigree you constructed in Part A. Based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? Based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? sex-linked dominant autosomal dominant sex-linked recessive autosomal recessive SubmitHintsMy AnswersGive UpReview Part Part C - Predicting the probability of inheritance Jane and John are considering having another child. Given the pedigree you constructed...
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) (2 pts) (b) In pedigree B, circle all individuals who are heterozygous. or to 0 0 - 이 SSO | 호 co | or - TTT Choices: A. Y-linked, B. X-linked dominant C. recessive, D. Autosomal dominant, E. Autosomal recessive.
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...
The mode of inheritance for this pedigree is autosomal dominant. If I-1 and II-2 were to have another child, what is the probability that their child would express the trait? Explain. 1 1 N II 1 3 4 5 6 N = 1 2 3 4 5 6
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
. O . Using Pedigrees to hypothesize patterns of inheritance 5. For each of the pedigree charts on the following page, determine which pattern of inheritance most likely explains the observed pattern of traits in the family shown. Observe the general patterns in the pedigree charts on the following page o males vs females? parents with disease? Compare these patterns with the clues on the previous page to hypothesize a pattern of inheritance Based on this pattern of inheritance, use...
also name mode of inheritance thx :) (b) In pedigree B, circle all individuals who are heterozygous. (2 pts) O Hoo-ooo SO SO 오 모오모오모 이 d 0 0 2 모 오모모모 1 오오모 | CAL M OOOOO TT
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