Recherche
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Spectrum of PTCH1 Mutations in French Patients with Gorlin Syndrome
(Journal of Investigative Dermatology. vol. 121, n° 3, pp. 478-481, 2003-09)Article de revue -
Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients
(European Journal of Human Genetics. vol. 15, n° 8, pp. 843-847, 2007-08)Article de revue -
Value of microsatellite instability typing in detecting hereditary non-polyposis colorectal cancer. A prospective multicentric study by the Association Aquitaine Gastro.
(Gastroentérologie Clinique et Biologique / Research and Clinics in Hepatology and Gastroenterology. vol. 29, n° 6-7, pp. 667-75, 2005)Article de revue -
Molecular Basis for Expression of Common and Rare Fragile Sites
(Molecular and Cellular Biology. vol. 23, n° 20, pp. 7143-7151, 2003-10-15)Article de revue