An inherited disease in a mom that affects all children regardless of sex, but then occurs in only and all granddaughters is likely to be caused by:
a. |
A mutation in a gene on a non-sex chromosome (autosome) |
|
b. |
A mutation in a gene located on the mitochondrial chromosome |
|
c. |
A mutation in a gene on the Y chromosome |
|
d. |
A mutation in a gene on the X chromosome |
ansr) A muation in a gene on the X chromosome.
normal father affected mother(HOMOZYGOUS)
FATHER/MOTHER | X | XY |
X | XX(Affected)(HETEROZYGOUS) | XY(Affected) |
X | XX(Affected)(HETEROZYGOUS) | XY(Affected) |
all are affected because of the one X linked dominant allele of the mother.
In the next generation,
Affected male normal female
male/female | X | Y |
X | XX(Females affected) | XY(NON AFFECTED MALE) |
X | XX(Female affected) | XY(NON AFFECTED MALE) |
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