| Literature DB >> 2754723 |
M S Bhate1, P E Robertson, E V Davison, J A Brummitt.
Abstract
A case of Prader Willi Syndrome who suffered from hypothyroidism is described. This patient on cytogenetic examination was found to have Mosaic 46,XX/46,XX,del(15)(q11.1q11.2) karyotype.Entities:
Mesh：
Year: 1989 PMID： 2754723 DOI： 10.1111/j.1365-2788.1989.tb01471.x
Source DB: PubMed Journal: J Ment Defic Res ISSN： 0022-264X