Complete the Punnett square below of a cross between a carrier mother (a female who carries one copy of the recessive allele and so appears normal herself) and a non-hemophiliac father. otier hand, has only one X chromosome, and so needs only one copy of the recessive allele to have the e 1. Drag the pink labels to the pink targets to indicate the sex dictated by the genotype in each box. (Pink labels may be used more than once.) 2. Drag the blue labels to the blue targets to indicate whether the genotype in each box confers hemophilia, normal, or carrier status. (Blue labels may be used more than once.) Reset Help x"x (carrier) mother x"Y (normal) father Sperm from father Y hemophilliac carrier XH Group 2 Group 2 normal Group 1 Group 1 female Eggs from mother male x"xh Group 2 Group 2 Group 1 Group 1
Complete the Punnett square below of a cross between a carrier mother (a female who carries one copy of the recessive allele and so appears normal herself) and a non-hemophiliac father. otier hand, has only one X chromosome, and so needs only one copy of the recessive allele to have the e 1. Drag the pink labels to the pink targets to indicate the sex dictated by the genotype in each box. (Pink labels may be used more than once.) 2. Drag the blue labels to the blue targets to indicate whether the genotype in each box confers hemophilia, normal, or carrier status. (Blue labels may be used more than once.) Reset Help x"x (carrier) mother x"Y (normal) father Sperm from father Y hemophilliac carrier XH Group 2 Group 2 normal Group 1 Group 1 female Eggs from mother male x"xh Group 2 Group 2 Group 1 Group 1
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Introduction:
Hemophilia is an X-linked recessive disorder that follows the pattern of mother to son. Females are affected only when they have both the X chromosomes affected, i.e. mother is a carrier and the father is a known hemophiliac. Then too they have a 50% chance of getting the disease and hence it is rarely seen in females.
Males with one X chromosome can not be carriers and are affected by the disease.
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