Annals of Human Genetics · 1962 · 46 citations · 19 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsHuman GeneticsMedical GeneticsChromosomal AbnormalitiesChromosomal DisordersChromosomal TranslocationsDown SyndromeGenetic DisordersGenetic LinkageInherited Chromosomal DisordersTranslocations
Summary A family has been described in which the transmission of a translocation between two chromosomes of the 13–15 group can be traced through at least three generations. All balanced translocation carriers are apparently normal. A close approximation of a 1:1 ratio of carriers: normal has been found in the offspring from such translocation carriers, and this is compared with published data for the transmission of a 15/21 translocation associated with Down's syndrome. There is no conclusive evidence for the occurrence of trisomy in the family. The data suggest the absence of close linkage between the translocation and the ABO, Rhesus, MNS, ‘P’ and Duffy blood‐group loci.
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MULTIPLE CONGENITAL ANOMALY CAUSED BY AN EXTRA AUTOSOME
Klaus Pätau, DavidW. Smith, Eeva Therman et al. · The Lancet · 1960 · 686 citations
CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILD
M. Fraccaro, K Kaijser, J. Lindsten · The Lancet · 1960 · 174 citations
Life Sciences, Genetics, Pediatrics +10
CHROMOSOMAL TRANSLOCATIONS IN MONGOLISM AND IN NORMAL RELATIVES
L. S. PENROSE, J. R. Ellis, JoyD.A. Delhanty · The Lancet · 1960 · 163 citations
CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISM
C.O. Carter, J.L. Hamerton, P. E. Polani et al. · The Lancet · 1960 · 128 citations