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Items: 3

1.

Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features.

Rafiq MA, Leblond CS, Saqib MA, Vincent AK, Ambalavanan A, Khan FS, Ayaz M, Shaheen N, Spiegelman D, Ali G, Amin-ud-Din M, Laurent S, Mahmood H, Christian M, Ali N, Fennell A, Nanjiani Z, Egger G, Caron C, Waqas A, Ayub M, Rasheed S, Forgeot d'Arc B, Johnson A, So J, Brohi MQ, Mottron L, Ansar M, Vincent JB, Xiong L.

BMC Med Genet. 2015 Jun 25;16:41. doi: 10.1186/s12881-015-0183-0.

2.

Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.

Noor A, Lionel AC, Cohen-Woods S, Moghimi N, Rucker J, Fennell A, Thiruvahindrapuram B, Kaufman L, Degagne B, Wei J, Parikh SV, Muglia P, Forte J, Scherer SW, Kennedy JL, Xu W, McGuffin P, Farmer A, Strauss J, Vincent JB.

Am J Med Genet B Neuropsychiatr Genet. 2014 Jun;165B(4):303-13. doi: 10.1002/ajmg.b.32232.

PMID:
24700553
3.

Screening of NLGN3 and NLGN4X genes in Thai children with autism spectrum disorder.

Mikhailov A, Fennell A, Plong-on O, Sripo T, Hansakunachai T, Roongpraiwan R, Sombuntham T, Ruangdaraganon N, Vincent JB, Limprasert P.

Psychiatr Genet. 2014 Feb;24(1):42-3. doi: 10.1097/YPG.0000000000000019. No abstract available.

PMID:
24362370

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