Familial occurrence of chromosome variant 17ph+
- 23 April 2008
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 12 (1) , 39-42
- https://doi.org/10.1111/j.1399-0004.1977.tb00898.x
Abstract
A structural chromosome variant 17ph+ was found in a high genetic risk family. The possibility of a causal connection between minor structural changes in the karyotype and congenital defects appearing in 1 member of the family, is considered.This publication has 11 references indexed in Scilit:
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