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The British Journal of Dermatology
|
September 8, 2011
Molecular genetic support for the rule of dichotomy in type 2 segmental Darier disease
R Fölster-Holst, R G L Nellen, J-M Jensen, et al.
Archives of Dermatology
|
February 1, 1996
Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency
M F Jonkman, M C de Jong, K Heeres, et al.
The Journal of Investigative Dermatology
|
July 1, 1985
Monoclonal antibodies selected to discriminate between malignant melanomas and nevocellular nevi
D J Ruiter, G M Dingjan, P M Steijlen, et al.
The British Journal of Dermatology
|
January 8, 2013
Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene
R G L Nellen, P M Steijlen, H C Hennies, et al.
The British Journal of Dermatology
|
October 24, 2007
Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome
P M Steijlen, M van Geel, M Vreeburg, et al.
Journal of Dermatological Science
|
November 1, 2011
A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome
J J A J van der Velden, M F Jonkman, W H I McLean, et al.
Brain : a Journal of Neurology
|
June 16, 2001
Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome
M A Willemsen, L IJlst, P M Steijlen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 26, 2018
CYLD mutations differentially affect splicing and mRNA decay in Brooke-Spiegler syndrome
L J M T Parren, J M Baron, S Joussen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 1, 2023
HRAS mosaicism in linear palmoplantar keratoderma
J M K Clabbers, G M J M Roemen, N Rajan, et al.
The Journal of Investigative Dermatology
|
August 1, 1996
RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasia
R M Hofstra, R H Sijmons, T Stelwagen, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 145) with videos related to
Sort By:
Page
of 15
The British Journal of Dermatology
|
September 8, 2011
Molecular genetic support for the rule of dichotomy in type 2 segmental Darier disease
R Fölster-Holst, R G L Nellen, J-M Jensen, et al.
Archives of Dermatology
|
February 1, 1996
Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency
M F Jonkman, M C de Jong, K Heeres, et al.
The Journal of Investigative Dermatology
|
July 1, 1985
Monoclonal antibodies selected to discriminate between malignant melanomas and nevocellular nevi
D J Ruiter, G M Dingjan, P M Steijlen, et al.
The British Journal of Dermatology
|
January 8, 2013
Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene
R G L Nellen, P M Steijlen, H C Hennies, et al.
The British Journal of Dermatology
|
October 24, 2007
Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome
P M Steijlen, M van Geel, M Vreeburg, et al.
Journal of Dermatological Science
|
November 1, 2011
A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome
J J A J van der Velden, M F Jonkman, W H I McLean, et al.
Brain : a Journal of Neurology
|
June 16, 2001
Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome
M A Willemsen, L IJlst, P M Steijlen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 26, 2018
CYLD mutations differentially affect splicing and mRNA decay in Brooke-Spiegler syndrome
L J M T Parren, J M Baron, S Joussen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 1, 2023
HRAS mosaicism in linear palmoplantar keratoderma
J M K Clabbers, G M J M Roemen, N Rajan, et al.
The Journal of Investigative Dermatology
|
August 1, 1996
RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasia
R M Hofstra, R H Sijmons, T Stelwagen, et al.
Page
of 15