Detalhe da pesquisa
1.
Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability.
Hum Mutat
; 34(1): 237-47, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23033313