Detalhe da pesquisa
1.
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.
Am J Med Genet A
; 155A(10): 2386-96, 2011 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-22031302
2.
IRF6 mutations in mixed isolated familial clefting.
Am J Med Genet A
; 152A(12): 3107-9, 2010 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-21082654
3.
Imperforate anus is a rare associated finding in blepharocheilodontic syndrome.
Am J Med Genet A
; 152A(2): 438-40, 2010 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-20101698
4.
Further delineation of the Kapur-Toriello syndrome.
Am J Med Genet A
; 152A(4): 1013-5, 2010 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-20358618