Detalhe da pesquisa
1.
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.
Nat Genet
; 38(9): 1032-7, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16906163
2.
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia.
Eur J Hum Genet
; 15(8): 898-901, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17406642