Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.

Source:http://linkedlifedata.com/resource/pubmed/id/4821173

N. Engl. J. Med. 1974 May 16 290 20 1097-103

Download in:

View as

General Info

PMID
4821173