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N Soufir

Showing results (11-20 of 28) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|November 28, 2017
Clinical and genetic characteristics of xeroderma pigmentosum in NepalP Espi, S Parajuli, M Benfodda, et al.
Human Molecular Genetics|March 21, 1998
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study GroupN Soufir, M F Avril, A Chompret, et al.
Clinical Genetics|August 1, 2014
Germline BAP1 mutations predispose also to multiple basal cell carcinomasA de la Fouchardière, O Cabaret, L Savin, et al.
Molecular Carcinogenesis|April 2, 2004
INK4a-ARF mutations in skin carcinomas from UV irradiated hairless miceN Soufir, S Queille, K Mollier, et al.
American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.
British Journal of Cancer|December 19, 2001
Divergence between the high rate of p53 mutations in skin carcinomas and the low prevalence of anti-p53 antibodiesC Moch, A Moysan, R Lubin, et al.
Revue De Stomatologie Et De Chirurgie Maxillo-Faciale|May 26, 2012
[Pediatric keratocystic odontogenic tumor and nevoid basal cell carcinoma syndrome. Predictive factors for recurrence and aggressiveness]N Kadlub, M-E Gatibelza, N El Houmami, et al.
The British Journal of Dermatology|February 16, 2007
Inactivation of the CDKN2A and the p53 tumour suppressor genes in external genital carcinomas and their precursorsN Soufir, S Queille, M Liboutet, et al.
The British Journal of Dermatology|August 23, 2008
Xeroderma pigmentosum group C in a French Caucasian patient with multiple melanoma and unusual long-term survivalS Jacobelli, N Soufir, J J Lacapere, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Journal of the European Academy of Dermatology and Venereology : JEADV|November 28, 2017
Clinical and genetic characteristics of xeroderma pigmentosum in NepalP Espi, S Parajuli, M Benfodda, et al.
Human Molecular Genetics|March 21, 1998
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study GroupN Soufir, M F Avril, A Chompret, et al.
Clinical Genetics|August 1, 2014
Germline BAP1 mutations predispose also to multiple basal cell carcinomasA de la Fouchardière, O Cabaret, L Savin, et al.
Molecular Carcinogenesis|April 2, 2004
INK4a-ARF mutations in skin carcinomas from UV irradiated hairless miceN Soufir, S Queille, K Mollier, et al.
American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.
British Journal of Cancer|December 19, 2001
Divergence between the high rate of p53 mutations in skin carcinomas and the low prevalence of anti-p53 antibodiesC Moch, A Moysan, R Lubin, et al.
Revue De Stomatologie Et De Chirurgie Maxillo-Faciale|May 26, 2012
[Pediatric keratocystic odontogenic tumor and nevoid basal cell carcinoma syndrome. Predictive factors for recurrence and aggressiveness]N Kadlub, M-E Gatibelza, N El Houmami, et al.
The British Journal of Dermatology|February 16, 2007
Inactivation of the CDKN2A and the p53 tumour suppressor genes in external genital carcinomas and their precursorsN Soufir, S Queille, M Liboutet, et al.
The British Journal of Dermatology|August 23, 2008
Xeroderma pigmentosum group C in a French Caucasian patient with multiple melanoma and unusual long-term survivalS Jacobelli, N Soufir, J J Lacapere, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
Pageof 3