Detalhe da pesquisa
1.
Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.
Pediatr Res
; 73(6): 772-6, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-23481551
2.
An unusual case of Cat-Eye syndrome phenotype and extragonadal mature teratoma: review of the literature.
Birth Defects Res A Clin Mol Teratol
; 94(7): 561-6, 2012 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-22730277
3.
Generation of human ß-thalassemia induced pluripotent cell lines by reprogramming of bone marrow-derived mesenchymal stromal cells using modified mRNA.
Cell Reprogram
; 16(6): 447-55, 2014 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-25354259
4.
Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism.
Psychiatr Genet
; 23(5): 198-203, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23851596
5.
Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation.
Eur J Paediatr Neurol
; 17(3): 316-20, 2013 May.
Artigo
Inglês
| MEDLINE | ID: mdl-23352671
6.
Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.
Gene
; 506(2): 360-8, 2012 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22766398