Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome.

Adult Blood Group Antigens Child Chromosome Aberrations Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Dermatoglyphics Down Syndrome/genetics Duodenal Obstruction/complications Female Heart Defects, Congenital/complications Humans Hyperbilirubinemia/complications Infant, Newborn Karyotyping Male Mitosis Mosaicism Pedigree Sex Chromosomes

Blood Group Antigens