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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 Nepal
P 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 Group
N Soufir, M F Avril, A Chompret, et al.
Clinical Genetics
|
August 1, 2014
Germline BAP1 mutations predispose also to multiple basal cell carcinomas
A de la Fouchardière, O Cabaret, L Savin, et al.
Molecular Carcinogenesis
|
April 2, 2004
INK4a-ARF mutations in skin carcinomas from UV irradiated hairless mice
N 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-q24
V 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 antibodies
C 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 precursors
N 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 survival
S 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 C
S Hadj-Rabia, D Oriot, N Soufir, et al.
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of 3
Search research articles
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Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 28, 2017
Clinical and genetic characteristics of xeroderma pigmentosum in Nepal
P 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 Group
N Soufir, M F Avril, A Chompret, et al.
Clinical Genetics
|
August 1, 2014
Germline BAP1 mutations predispose also to multiple basal cell carcinomas
A de la Fouchardière, O Cabaret, L Savin, et al.
Molecular Carcinogenesis
|
April 2, 2004
INK4a-ARF mutations in skin carcinomas from UV irradiated hairless mice
N 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-q24
V 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 antibodies
C 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 precursors
N 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 survival
S 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 C
S Hadj-Rabia, D Oriot, N Soufir, et al.
Page
of 3