M. Isnard

Prenatal Three-Dimensional Ultrasound Detection of Adducted Thumbs in X-Linked Hydrocephaly: Two Case Reports with Molecular Genetic Studies

P. Saugier-Veber, W. Sepulveda, E. Corral, 2015, Case reports in obstetrics and gynecology.

Osteosclerotic bone dysplasia in siblings with a Fam20C mutation

Corinne Stoetzel, Jean Muller, Meriam Koob, 2011, Clinical genetics.

Successful Intrauterine Therapy for Congenital Cystic Adenomatoid Malformation of the Lung

R. Favre, C. Vayssière, M. Kohler, 2007, Fetal Diagnosis and Therapy.

Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation Sequencing.

J. Millán, J. Roume, J. Salles, 2015, Molecular genetics and metabolism.

Menstrual toxic shock syndrome: a French nationwide multicenter retrospective study.

G. Lina, P. Kalfon, P. Asfar, 2021, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.