Detalhe da pesquisa
1.
De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity.
Genet Med
; 26(5): 101087, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38288683
2.
Is laterality of congenital diaphragmatic hernia a reliable prognostic factor? French national cohort study.
Prenat Diagn
; 40(8): 949-957, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32279384
3.
Prenatal therapy with pyrimethamine + sulfadiazine vs spiramycin to reduce placental transmission of toxoplasmosis: a multicenter, randomized trial.
Am J Obstet Gynecol
; 219(4): 386.e1-386.e9, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-29870736
4.
Ex utero intrapartum technique (EXIT): Indications, procedure methods and materno-fetal complications - A literature review.
J Gynecol Obstet Hum Reprod
; 51(1): 102252, 2022 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-34638008
5.
Prenatal diagnosis of Desbuquois dysplasia type 1 by whole exome sequencing before the occurrence of specific ultrasound signs.
J Matern Fetal Neonatal Med
; 34(13): 2217-2220, 2021 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-31510824
6.
Medical Termination Of Pregnancy For Psychosocial Reasons.
J Gynecol Obstet Hum Reprod
; 50(6): 101932, 2021 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-33031946
7.
Management of fetal goiters: 6-year retrospective observational study in three prenatal diagnosis and treatment centers of the Pays De Loire Perinatal Network.
J Matern Fetal Neonatal Med
; 33(15): 2561-2569, 2020 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-30513035
8.
Pregnancy outcome in Turner syndrome: A French multi-center study after the 2009 guidelines.
Eur J Obstet Gynecol Reprod Biol
; 229: 20-25, 2018 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-30096465
9.
Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2.
Prenat Diagn
; 24(10): 828-32, 2004 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-15503273
10.
Absence of deletion at the SOX2 locus in a case of microphthalmia and esophageal atresia.
Am J Med Genet A
; 131(2): 204, 2004 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-15487011