Laurent Bidat

6 Av De L'Ile De France
Pontoise, 95300, France

Last Updated: 09/26/2026

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Found 10 publications

Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies.

Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies.

Journal: Journal of clinical medicine

Published: July 08, 2020

Impact of simulation-based prenatal invasive procedure training on professional practice, a preliminary study.

Impact of simulation-based prenatal invasive procedure training on professional practice, a preliminary study.

Journal: Journal of gynecology obstetrics and human reproduction

Published: July 01, 2020

Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.

Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.

Journal: Kidney international

Published: April 22, 2020

Cell-free fetal DNA versus maternal serum screening for trisomy 21 in pregnant women with and without assisted reproduction technology: a prospective interventional study.

Cell-free fetal DNA versus maternal serum screening for trisomy 21 in pregnant women with and without assisted reproduction technology: a prospective interventional study.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 11, 2017

WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.

WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.

Journal: Brain : a journal of neurology

Published: February 27, 2017

Teaching invasive prenatal procedures: effectiveness of two simple simulators in training.

Teaching invasive prenatal procedures: effectiveness of two simple simulators in training.

Journal: Prenatal diagnosis

Published: March 08, 2016

De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathy.

De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathy.

Journal: European journal of medical genetics

Published: July 17, 2015

Cell-free DNA analysis in maternal plasma in cases of fetal abnormalities detected on ultrasound examination.

Cell-free DNA analysis in maternal plasma in cases of fetal abnormalities detected on ultrasound examination.

Journal: Obstetrics and gynecology

Published: May 23, 2015

Performance and indications of noninvasive prenatal testing using cell free circulating fetal DNA (cffDNA) for the detection of fetal trisomy 21, 18 and 13 in France

Performance and indications of noninvasive prenatal testing using cell free circulating fetal DNA (cffDNA) for the detection of fetal trisomy 21, 18 and 13 in France

Journal: Journal de gynecologie, obstetrique et biologie de la reproduction

Published: April 24, 2015

Chorionic villus sampling training method

Chorionic villus sampling training method

Journal: Journal de gynecologie, obstetrique et biologie de la reproduction

Published: January 03, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026