Laetitia Gaillard

Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability

Tangui Le Guen, Laurent Jullien, Fabien Touzot et al. · Human Molecular Genetics · 2013 · 191 citations · Full text

Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal–Hreidarsson syndrome

Fabien Touzot, Isabelle Callebaut, Jean Soulier et al. · Proceedings of the National Academy of Sciences · 2010 · 87 citations · Full text

Primary Microcephaly, Impaired DNA Replication, and Genomic Instability Caused by Compound Heterozygous<i>ATR</i>Mutations

Houda Benhelli‐Mokrani, Laetitia Gaillard, Patricia Biasutto et al. · Human Mutation · 2012 · 55 citations

Genetics, Genomic Mechanism, Molecular Genetics +17

Heterogeneous telomere defects in patients with severe forms of dyskeratosis congenita

Fabien Touzot, Laetitia Gaillard, Nadia Vasquez et al. · Journal of Allergy and Clinical Immunology · 2011 · 41 citations

Genetic Disorder, Medicine, Dyskeratosis Congenita +3