Detalles de la búsqueda
1.
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).
Hum Mol Genet
; 21(16): 3647-54, 2012 Aug 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22619378
2.
C1q but not mannose-binding lectin (Mbl-2) gene polymorphisms are associated with type 2 diabetes in the genetically homogeneous population of the island of Crete in Greece.
Hum Immunol
; 74(7): 878-81, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23602874
Resultados
1 -
2
de 2
1
Próxima >
>>