18.Roberts Syndrome is an extremely rare genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, legs. Shown below is a pedigree for a family with Roberts Syndrome. Consider couple Il-C and Il-D. What is the probability that their next two children will have Roberts Syndrome? and A C D || A C D F II А А. 1/4 В. 1/16 C. Insufficient data D. %

Human Anatomy & Physiology (11th Edition)
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18. Please answer
18.Roberts Syndrome is an extremely rare genetic disorder that is
characterized by mild to severe prenatal retardation or disruption of cell
division, leading to malformation of the bones in the skull, face, arms, and
legs. Shown below is a pedigree for a family with Roberts Syndrome. Consider
couple Il-C and Il-D. What is the probability that their next two children will
have Roberts Syndrome?
A
B
C
D
||
A
C
D
F
II
A
В
А. 1/4
В. 1/16
C. Insufficient data
D. V%
Transcribed Image Text:18.Roberts Syndrome is an extremely rare genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, and legs. Shown below is a pedigree for a family with Roberts Syndrome. Consider couple Il-C and Il-D. What is the probability that their next two children will have Roberts Syndrome? A B C D || A C D F II A В А. 1/4 В. 1/16 C. Insufficient data D. V%
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