In a human genetic study, a family with five phenotypically normal children
was investigated. Two children were "homozy. gous" for a Robertsonian
translocation between chromosomes 19 and 20 (they contained two identical
copies of the fused chromosome). They have only 44 chromosomes but a complete
genetic complement. Three of the children were "heterozygous" for the
translocation and contained 45 chromosomes, with one translocated chromosome
plus a normal copy of both chromosomes 19 and \(20 .\) Two other pregnancies
resulted in stillbirths. It was later discovered that the parents were first
cousins. Based on this information, determine the chromosome compositions of
the parents. What led to the stillbirths? Why was the discovery that the
parents were first cousins a key piece of information in understanding the
genetics of this family?