Detalhe da pesquisa
1.
Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome.
Nat Genet
; 38(5): 561-5, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16642020
2.
Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing Heritability.
G3 (Bethesda)
; 8(9): 2881-2888, 2018 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-30166421
3.
Host genetic risk factors for West Nile virus infection and disease progression.
PLoS One
; 6(9): e24745, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21935451
4.
Clinical characteristics and natural history of Freeman-Sheldon syndrome.
Pediatrics
; 117(3): 754-62, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16510655
5.
Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes.
Am J Hum Genet
; 72(3): 681-90, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12592607
6.
Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype.
Am J Hum Genet
; 73(1): 74-85, 2003 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12789647