
doi: 10.1007/bf00273332
pmid: 50273
The present study describes 2 cases of a balanced reciprocal translocation in the C-group of autosomes. Familial translocation 46,XX,t(6;7) was found both in a woman cytogenetically examined because of a developmental anomaly of the internal genitals (uterus bicornis subseptus) and in her healthy mother. Chromosomal complement 46,XYt(8;10) was proved in the healthy father of a child showing clinical features of Down's syndrome with a karyotype 47,XY,21+. Q- and G-banding techniques were used for precise identification of the chromosomes involved in translocations.
Adult, Chromosome Aberrations, Chromosomes, Human, 6-12 and X, Male, Staining and Labeling, Uterus, Infant, Translocation, Genetic, Pedigree, Humans, Female, Down Syndrome
Adult, Chromosome Aberrations, Chromosomes, Human, 6-12 and X, Male, Staining and Labeling, Uterus, Infant, Translocation, Genetic, Pedigree, Humans, Female, Down Syndrome
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