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1.
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes.
Am J Med Genet A
; 167A(11): 2555-62, 2015 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-26129644
2.
Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene.
Pediatr Dermatol
; 31(1): 83-7, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24015686
3.
Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair.
Exp Dermatol
; 21(6): 469-71, 2012 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-22621192
4.
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss.
Arch Dermatol Res
; 305(3): 249-53, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23124548
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