Annaig Briand

Disruption of the SEMA3D Gene in a Patient with Congenital Heart Defects

V. Gournay, O. Pichon, A. David, 2015, Human mutation.

De novo duplication and deletions at 7q in a three‐generation family

L. Pérez-Jurado, C. Le Caignec, B. Isidor, 2012, American journal of medical genetics. Part A.

Wilms’ tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas

O. Delattre, N. Sevenet, C. Jeanpierre, 2012, European Journal of Human Genetics.

Autosomal insertional translocation mimicking an X-linked mode of inheritance.

C. Le Caignec, O. Pichon, A. David, 2013, European journal of medical genetics.

Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster

R. Redon, D. Duboule, A. Mégarbané, 2019, European Journal of Human Genetics.

Mandibular dysostosis without microphthalmia caused by OTX2 deletion

C. Le Caignec, B. Isidor, O. Pichon, 2016, American journal of medical genetics. Part A.