| Literature DB >> 1781956 |
P Petit1, P Moerman, J P Fryns.
Abstract
A 20 weeks gestation female fetus with a lobar holoprosencephaly and Xq22 deletion is described. The phenotype correlation of the cerebral defect with the facial features is positive. On the contrary phenotypic-karyotypic correlation is non obvious.Entities:
Mesh：
Year: 1991 PMID： 1781956
Source DB: PubMed Journal: Genet Couns ISSN： 1015-8146