| Literature DB >> 891007 |
Abstract
A structural chromosome variant 17ph+ was found in a high genetic risk family. The authors consider the possibility of a causal connection between minor structural changes in the karyotype and congenital defects appearing in one member of the family.Entities:
Mesh：
Year: 1977 PMID： 891007 DOI： 10.1111/j.1399-0004.1977.tb00898.x
Source DB: PubMed Journal: Clin Genet ISSN： 0009-9163 Impact factor: 4.438