Structural heterozygosis in man: analysis of two families
作者： J. H. EDWARDS , M. FRACCARO , PAMELA DAVIES , R. B. YOUNG , L. S. PENROSE
DOI: 10.1111/J.1469-1809.1962.TB01323.X
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摘要: Summary Two families are described in each of which the father is presumed to have an autosomal reciprocal translocation as a result both children one family, and three other, grossly abnormal. The translocations probably between chromosomes nos. 9 4 first 1 6 second family. abnormalities karyotype regarded examples duplication deficiencies. Unusual dermal ridge patterns were observed individuals with abnormal karyotypes.
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