1. Mr. and Ms. B have a child with three copies of chromosome 21. The child has a chromo- somal abnormality known as 2. This abnormality, like any change in DNA, is known as a(n) 3. Chromosome 21 is one of 22 pairs of chromosomes known as 4. The remainder of the child’s chromosomes are normal. The total number of chromosomes in the child’s cells is 5. The chromosome abnormality arose during the production of gametes. The form of cell divi. sion that occurs exclusively in germ cell precursors is called 6. The family knew in advance about their baby’s chromosome abnormality because of prenatal screening and testing. The first indication was an abnormal accumulation of fluid at the back of the fetus’s neck. This test, which uses ultrasound, is known as the. Get Medicine Homework Help Today
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