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R C Betz

Showing results (1-10 of 38) with videos related to

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The British Journal of Dermatology|October 21, 2017
A path through the reticulate pigmentation disorder jungleR C Betz
The British Journal of Dermatology|July 25, 2019
Novel mutation for disseminated superficial actinic porokeratosis and its functional impact at the protein levelR C Betz
The British Journal of Dermatology|October 30, 2015
Nails - more than just an ectodermal appendage: the genetics behind isolated nail disordersR C Betz
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 6, 2014
[Alopecia and hypotrichosis in childhood: clinical features and diagnosis]R C Betz
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 15, 2019
[Hair anomalies in syndromic disorders]J Frank, R C Betz
The British Journal of Dermatology|March 2, 2013
Autosomal recessive isolated familial acanthosis nigricans in a Pakistani family due to a homozygous mutation in the insulin receptor geneS Ahmad, H Mahmoudi, M Naeem, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 27, 2022
Cole disease due to a novel pathogenic variant in the ENPP1 geneA Nanda, X Xiong, A AlLafi, et al.
The British Journal of Dermatology|May 30, 2012
Steatocystoma multiplex: keratin 17 - the key player?A S Antal, D Kulichova, S Redler, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 25, 2021
Atrichia with papular lesions: a differential diagnosis of alopecia universalis not to be missedA Ibrahim, F Buket Basmanav, G Bohelay, et al.
Clinical and Experimental Dermatology|January 9, 2010
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosisS Düzenli, S Redler, M Müller, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
The British Journal of Dermatology|October 21, 2017
A path through the reticulate pigmentation disorder jungleR C Betz
The British Journal of Dermatology|July 25, 2019
Novel mutation for disseminated superficial actinic porokeratosis and its functional impact at the protein levelR C Betz
The British Journal of Dermatology|October 30, 2015
Nails - more than just an ectodermal appendage: the genetics behind isolated nail disordersR C Betz
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 6, 2014
[Alopecia and hypotrichosis in childhood: clinical features and diagnosis]R C Betz
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 15, 2019
[Hair anomalies in syndromic disorders]J Frank, R C Betz
The British Journal of Dermatology|March 2, 2013
Autosomal recessive isolated familial acanthosis nigricans in a Pakistani family due to a homozygous mutation in the insulin receptor geneS Ahmad, H Mahmoudi, M Naeem, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 27, 2022
Cole disease due to a novel pathogenic variant in the ENPP1 geneA Nanda, X Xiong, A AlLafi, et al.
The British Journal of Dermatology|May 30, 2012
Steatocystoma multiplex: keratin 17 - the key player?A S Antal, D Kulichova, S Redler, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 25, 2021
Atrichia with papular lesions: a differential diagnosis of alopecia universalis not to be missedA Ibrahim, F Buket Basmanav, G Bohelay, et al.
Clinical and Experimental Dermatology|January 9, 2010
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosisS Düzenli, S Redler, M Müller, et al.
Pageof 4