Yvan Herenger

发表

AnnotSV: an integrated tool for structural variations annotation

Véronique Geoffroy, Amélie Piton, Corinne Stoetzel, 2018, Bioinform..

20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

Claire Redin, Jean Muller, Laurence Faivre, 2013, European Journal of Human Genetics.

Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing

Véronique Geoffroy, Claire Redin, Jean Muller, 2014, Journal of Medical Genetics.