Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly.
作者信息
Madan K, Lindhout D, Palan A
机构信息
Institute of Human Genetics, Medical Faculty, Free University, Amsterdam, The Netherlands.
出版信息
Hum Genet. 1987 Oct;77(2):193-6. doi: 10.1007/BF00272391.
PMID:3653892
Abstract
We describe a family with an increased frequency of cells with premature centromere division (PCD) of all chromosomes in four phenotypically normal individuals. This familial PCD phenomenon is apparently different from the well-described PCD of the X chromosome and from the centromere splitting in cells of patients with Roberts syndrome. Implications for genetic counseling are discussed.
摘要
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