Detalhe da pesquisa
1.
Morphological and genetic causes of fetal cardiomyopathies.
Clin Genet
; 104(1): 63-72, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37209000
2.
Multiple wavelength (365-475 nm) complete actinometric characterization of Corning® Lab Photo Reactor using azobenzene as a highly soluble, cheap and robust chemical actinometer.
Photochem Photobiol Sci
; 21(3): 421-432, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35147919
3.
Selective photoredox direct arylations of aryl bromides in water in a microfluidic reactor.
Org Biomol Chem
; 19(13): 3016-3023, 2021 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33885555
4.
Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype?
Clin Genet
; 98(6): 620-621, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32926417
5.
Fetal megacystis-microcolon: Genetic mutational spectrum and identification of PDCL3 as a novel candidate gene.
Clin Genet
; 98(3): 261-273, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32621347
6.
Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomalies.
Am J Med Genet A
; 176(5): 1091-1098, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29681083
7.
Corpus Callosum Abnormalities and Short Femurs in Beckwith-Wiedemann Syndrome: A Report of Two Fetal Cases.
Fetal Pediatr Pathol
; 37(6): 411-417, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30595068
8.
Efficiency of prenatal diagnosis in Pierre Robin sequence.
Prenat Diagn
; 37(11): 1169-1175, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28950416
9.
A French Approach to Test Fetuses with Ultrasound Abnormalities Using a Customized Microarray as First-Tier Genetic Test.
Cytogenet Genome Res
; 147(2-3): 103-10, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26735902
10.
Prenatal-onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation.
Birth Defects Res
; 113(18): 1324-1332, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34491000
11.
Prenatal diagnosis of a fetal abdominal eventration: a rare congenital abdominal wall defect.
Fetal Diagn Ther
; 23(2): 117-20, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18046068
12.
Formation of quaternary centers by copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents.
Angew Chem Int Ed Engl
; 52(31): 7995-9, 2013 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-23780788
13.
Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1.
Birth Defects Res
; 110(6): 538-542, 2018 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29316359
14.
In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses.
Birth Defects Res
; 110(4): 382-389, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29193896
15.
Fetal Cerebral Ventricular Dilatation: Etiopathogenic Study of 130 Observations.
Birth Defects Res
; 109(19): 1586-1595, 2017 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28758373
16.
French multicentric survey of outcome of pregnancy in women with pregestational diabetes.
Diabetes Care
; 26(11): 2990-3, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14578228
17.
Enantioselective copper(I)-phosphoramidite catalyzed addition of alkylzirconium species to acyclic enones.
Org Lett
; 17(4): 912-5, 2015 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25634651
18.
Copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents to cyclic enones to form quaternary centers.
Nat Protoc
; 9(1): 104-11, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24336474
19.
Asymmetric conjugate addition of alkylzirconium reagents to α,ß-unsaturated lactones.
Org Lett
; 16(12): 3288-91, 2014 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-24893570
20.
Hydrometallation-asymmetric conjugate addition: application to complex molecule synthesis.
Chem Commun (Camb)
; 49(39): 4211-3, 2013 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23192003