Detalhe da pesquisa
1.
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lancet
; 393(10173): 747-757, 2019 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30712880
2.
Immunocytochemical detection of ERG expression in exfoliated urinary cells identifies with high specificity patients with prostate cancer.
BJU Int
; 117(4): 686-96, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26471473
3.
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
Eur J Hum Genet
; 16(1): 18-27, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17940555
4.
14q22.3 Microdeletion encompassing OTX2 in a five-generation family with microphthalmia, pituitary abnormalities, and intellectual disability.
Ophthalmic Genet
; 37(3): 352-3, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26860946