Alain Martin

Fetal phenotype associated with the 22q11 deletion

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

Complete lung agenesis caused by complex genomic rearrangements with neo-TAD formation at the SHH locus

S. Mundlos, M. Spielmann, M. Holtgrewe, 2021, Human Genetics.

Contribution of BRCA1 and BRCA2 germ‐line mutations to the incidence of breast cancer in young women: Results from a prospective population‐based study in France

D. Easton, A. Antoniou, G. Lenoir, 2005, Genes, chromosomes & cancer.

Prognosis of early-onset breast cancer based on BRCA1/2 mutation status in a French population-based cohort and review

N. Voirin, G. Lenoir, I. Treilleux, 2006, Breast Cancer Research and Treatment.