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1.
Exome sequencing identifies the first genetic determinants of sirenomelia in humans.
Hum Mutat
; 41(5): 926-933, 2020 05.
Article
in English
| MEDLINE | ID: mdl-32058622
2.
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.
Article
in English
| MEDLINE | ID: mdl-29870736
3.
Impact of prenatal diagnosis on the outcome of patients with a transposition of great arteries: A 24-year population-based study.
Birth Defects Res A Clin Mol Teratol
; 106(3): 178-84, 2016 Mar.
Article
in English
| MEDLINE | ID: mdl-26690971
4.
Prenatal Screening of 21 Microdeletion/Microduplication Syndromes and Subtelomeric Imbalances by MLPA in Fetuses with Increased Nuchal Translucency and Normal Karyotype.
Cytogenet Genome Res
; 146(1): 28-32, 2015.
Article
in English
| MEDLINE | ID: mdl-26201711
5.
Prenatal diagnosis of the VACTERL association using routine ultrasound examination.
Birth Defects Res A Clin Mol Teratol
; 103(10): 880-6, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26033534
6.
False positive morphologic diagnoses at the anomaly scan: marginal or real problem, a population-based cohort study.
BMC Pregnancy Childbirth
; 14: 112, 2014 Mar 24.
Article
in English
| MEDLINE | ID: mdl-24655605
7.
Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.
Birth Defects Res A Clin Mol Teratol
; 97(12): 806-11, 2013 Dec.
Article
in English
| MEDLINE | ID: mdl-24343879
8.
Analysis of the cost effectiveness of different strategies for the antenatal diagnosis of chromosomal aberrations in cases of ultrasound-identified fetal abnormalities.
Ann Biol Clin (Paris)
; 78(5): 483-491, 2020 Oct 01.
Article
in English
| MEDLINE | ID: mdl-32933889
9.
Normal intellectual skills in patients with Rhombencephalosynapsis.
Eur J Paediatr Neurol
; 29: 92-100, 2020 Nov.
Article
in English
| MEDLINE | ID: mdl-33046393
10.
Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies.
J Clin Med
; 9(8)2020 Aug 01.
Article
in English
| MEDLINE | ID: mdl-32752152
11.
Laryngotracheoesophageal cleft, a rare differential diagnosis of esophageal atresia.
J Gynecol Obstet Hum Reprod
; 47(10): 577-579, 2018 Dec.
Article
in English
| MEDLINE | ID: mdl-30232040
12.
Simultaneous, congenital, mucocoele of the Blandin-Nühn glands and teratoma of the tongue: early management and follow up at one year.
Br J Oral Maxillofac Surg
; 55(7): 724-726, 2017 Sep.
Article
in English
| MEDLINE | ID: mdl-28624163
13.
Congenital unilateral renal agenesis: Prevalence, prenatal diagnosis, associated anomalies. Data from two birth-defect registries.
Birth Defects Res
; 109(15): 1204-1211, 2017 Sep 01.
Article
in English
| MEDLINE | ID: mdl-28722320
14.
The changes in angiogenic gene expression in recurrent multiple chorioangiomas.
Fetal Diagn Ther
; 22(3): 161-8, 2007.
Article
in English
| MEDLINE | ID: mdl-17228150
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