Detalhe da pesquisa
1.
Individual common variants exert weak effects on the risk for autism spectrum disorders.
Hum Mol Genet
; 21(21): 4781-92, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22843504
2.
Considerations regarding maintenance therapy for acute myeloid leukemia in remission.
Expert Rev Anticancer Ther
; 24(1-2): 15-20, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38230741
3.
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
PLoS Genet
; 5(6): e1000536, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19557195
4.
A unified genetic theory for sporadic and inherited autism.
Proc Natl Acad Sci U S A
; 104(31): 12831-6, 2007 Jul 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-17652511
5.
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.
Am J Hum Genet
; 71(4): 959-63, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12187510