Detalhe da pesquisa
1.
Effectiveness and costs of non-invasive foetal RHD genotyping in rhesus-D negative mothers: a French multicentric two-arm study of 850 women.
BMC Pregnancy Childbirth
; 18(1): 496, 2018 Dec 14.
Artigo
Inglês
| MEDLINE | ID: mdl-30547830
2.
Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway.
Hum Mutat
; 37(12): 1329-1339, 2016 12.
Artigo
Inglês
| MEDLINE | ID: mdl-27363716
3.
NEK1 and DYNC2H1 are both involved in short rib polydactyly Majewski type but not in Beemer Langer cases.
J Med Genet
; 49(4): 227-33, 2012 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-22499340
4.
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.
Hum Mutat
; 33(2): 316-26, 2012 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-22095942
5.
Three-dimensional ultrasound prenatal diagnosis of congenital ichthyosis: contribution of molecular biology.
Prenat Diagn
; 32(5): 498-500, 2012 May.
Artigo
Inglês
| MEDLINE | ID: mdl-22495968
6.
Circulating microRNAs as clinical biomarkers in the predictions of pregnancy complications.
Biomed Res Int
; 2015: 294954, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25699269
7.
Enhanced prevalence of plasmatic soluble MHC class I chain-related molecule in vascular pregnancy diseases.
Biomed Res Int
; 2014: 653161, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25243172
8.
Fetal RhD genotyping by real time quantitative PCR in maternal plasma of RhD-negative pregnant women from the Sahel of Tunisia.
Ann Biol Clin (Paris)
; 70(6): 683-8, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23207814