Recherche
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Etude clinique de mutations germinales du gène PTCH dans une série de 22 malades atteints du Syndrome de Gorlin
(Annales de Dermatologie et de Vénéréologie. vol. 133, n° 2, 2006)Article de revue -
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 -
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 -
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma
(British Journal of Cancer. vol. 99, n° 2, pp. 364-370, 2008-07)Article de revue -
Gorlin syndrome presenting as prenatal chylothorax in a girl
(Prenatal Diagnosis. vol. 25, n° 11, pp. 997-999, 2005-11)Article de revue -
Heterozygous mutations in the tumor suppressor gene PATCHED provoke basal cell carcinoma-like features in human organotypic skin cultures
(Oncogene. vol. 27, n° 51, pp. 6601-6606, 2008-10)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 -
Proteolipidic Vectors for Gene Transfer to the Lung
(Biochemical and Biophysical Research Communications. vol. 290, n° 5, pp. 1489-1498, 2002-02)Article de revue -
Limited specificity and large overlap of the functions of the mouse RARγ1 and RARγ2 isoforms
(Mechanisms of Development. vol. 66, n° 1-2, pp. 131-142, 1997-08)Article de revue -
Expression of p21 WAF1/CIP1 during mouse odontogenesis
(European Journal of Oral Sciences. vol. 106, n° S1, pp. 104-111, 1998-01)Article de revue