E. Alanio

Fetal phenotype associated with the 22q11 deletion

A. Laquérriere, R. Bouvier, L. Loeuillet, 2014, American journal of medical genetics. Part A.

Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita.

W. Talbot, J. Melki, G. Ravenscroft, 2015, American journal of human genetics.

Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.

C. Fallet-Bianco, D. Figarella-Branger, A. Laquérriere, 2012, Brain : a journal of neurology.

Characteristics and outcome of fetal cystic hygroma diagnosed in the first trimester

D. Gaillard, G. Ducarme, F. Vitry, 2007, Acta obstetricia et gynecologica Scandinavica.

Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations

R. Touraine, J. Mandel, J. Thevenon, 2020, Journal of Medical Genetics.

Recurrent prenatally diagnosed isolated bilateral pulmonary agenesis

R. Ramanah, D. Gaillard, D. Riethmuller, 2012, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The most important differential diagnoses to exclude are congenital diaphragmatic hernia , cystic adenomatous malformation and pulmonary sequestration

D. Gaillard, D. Riethmuller, F. Arbez-Gindre, 2012 .

Molecular heterogeneity in fetal forms of type II lissencephaly

M Joubert, C. Fallet-Bianco, D. Figarella-Branger, 2007, Human mutation.

[Gastroschisis: Prenatal ultrasonography and obstetrical criteria for predicting neonatal outcome].

E. Alanio, S. Bonneau, J. Bory, 2016, Gynecologie, obstetrique & fertilite.

Wernicke encephalopathy complicating hyperemesis gravidarum: a case report.

O. Graesslin, E. Bois, E. Alanio, 2010, European journal of obstetrics, gynecology, and reproductive biology.