| Literature DB >> 3653892 |
K Madan1, D Lindhout, A Palan.
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.Entities:
Mesh:
Year: 1987 PMID: 3653892 DOI: 10.1007/BF00272391
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132