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WGU D115 OBJECTIVE ASSESSMENT (OA) EXAM COMPLETE UNIT 1-UNIT 7 QUESTIONS AND CORRECT DETAILED ANSWERS Questions and Correct Answers/ Latest Update / Already Graded

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WGU D115 OBJECTIVE ASSESSMENT (OA) EXAM COMPLETE UNIT 1-UNIT 7 QUESTIONS AND CORRECT DETAILED ANSWERS Questions and Correct Answers/ Latest Update / Already Graded

Institution
WGU D115
Course
WGU D115

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WGU D115 OBJECTIVE ASSESSMENT (OA)
EXAM 2025-2026 COMPLETE UNIT 1-UNIT
7 QUESTIONS AND CORRECT DETAILED
ANSWERS Questions and Correct
Answers/ Latest Update / Already
Graded

Which type of genetic disease affects males more frequently than

females?




Sex-linked recessive


Autosomal recessive


Autosomal dominant


Sex-linked dominant


Ans: Sex-Linked recessive. Since males only have one X and one Y, if the

affected chromosome has the illness, it will be expressed.

,2|Page

In which two conditions are chromosomal abnormalities the leading

known cause?




Intellectual disability


Respiratory disorders


Fetal miscarriage


Cardiovascular disease


Mental illness


Check My Answer


Ans: Intellectual disability and fetal miscarriage. Chromosome

abnormalities are the leading known cause of intellectual disability and

fetal miscarriage.




What are three examples of prenatal diagnostic studies?


Drug-sensitivity testing


Chorionic villus sampling (CVS)

, 3|Page

Microscopy of cervical mucosa


Preimplantation genetic testing (PGT)


Amniocentesis


Ans: Chorionic villus sampling (CVS), amniocentesis, and preimplantation

genetic testing (PGT) are examples of prenatal diagnostic studies and are

performed in vitro. CVS is a form of genetic testing that provides genetic

information found in utero and is usually performed between weeks 11

and 14 of pregnancy. An amniocentesis is a form of genetic testing that

evaluates amniotic fluid and is usually performed during the second

trimester, between weeks 15 and 20 of pregnancy. PGT is performed on

the embryo prior to implantation.




Which genetic disorder is characterized by the presence of a zygote

having one chromosome with a normal complement of genes and

one chromosome with a missing gene?


Klinefelter syndrome


Down syndrome

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