Detalhe da pesquisa
1.
Additional evidence to support the role of the 20q13.33 region in susceptibility to autism.
Am J Med Genet A
; 161A(6): 1505-7, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23613186
2.
Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'.
Eur J Hum Genet
; 15(4): 446-52, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17290276