Detalhe da pesquisa
1.
Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex.
Clin Chem
; 62(6): 848-55, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27117469
2.
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies.
Genes (Basel)
; 15(1)2024 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38255008
3.
Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of ß-thalassaemia.
PLoS One
; 13(7): e0200348, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30044883
4.
Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.
Biomed Res Int
; 2013: 346762, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23555083
5.
Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations.
Mol Cytogenet
; 3: 24, 2010 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21110858