Detalhe da pesquisa
1.
Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-MB deletion of 14q12âq21.2 and a 550-KB deletion of 18p11.23: microarray delineation of an unbalanced chromosome rearrangement and a literature review.
Genet Couns
; 27(2): 165-76, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-29485807
2.
Clericuzio-type Poikiloderma with Neutropenia Syndrome in a Turkish Family: a Three Report of Siblings with Mutation in the C16orf57 gene.
Iran J Allergy Asthma Immunol
; 14(3): 331-7, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26546903
3.
Sternal closure with resorbable synthetic loop suture material in children.
J Pediatr Surg
; 35(9): 1309-11, 2000 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-10999685