Recherche
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MLH1 and MSH2 protein immunohistochemistry is useful for detection of hereditary non-polyposis colorectal cancer in young patients
(Histopathology. vol. 39, n° 3, pp. 250-258, 2001-09)Article de revue -
Mutation in exon 7 of PTCH deregulates SHH/PTCH/SMO signaling: Possible linkage to WNT
(International Journal of Molecular Medicine, 2006-05-01)Article de revue -
La dysplasie cléido-crânienne : attitudes thérapeutiques et recommandations. À propos d'une observation clinique
(Actualités Odonto-Stomatologiques. n° 247, pp. 241-254, 2009-09)Article de revue -
COL4A1 mutation in Axenfeld-Rieger anomaly with leukoencephalopathy and stroke
(Annals of Neurology. vol. 62, n° 2, pp. 177-184, 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 -
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