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Showing results (31-40 of 90) with videos related to

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Journal of Cellular and Molecular Medicine|June 18, 2002
Genetic analysis of factor V Leiden in a family with history of thrombosis and venous leg ulcersLucia M. Procopciuc, C. Has, C. Drugan, et al.
The British Journal of Dermatology|September 21, 2011
Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutationB Burger, I Spoerri, M Schubert, et al.
Annales De Dermatologie Et De Venereologie|January 29, 1999
[Multiple cutaneous cylindromas associated with parotid and submandibular gland cylindromas]A Baican, C Has, C Crisan, et al.
Clinical and Experimental Dermatology|June 11, 2013
Epidermolysis bullosa simplex: greater penetrance due to a keratin 5 gene variantM Jantke, C Has, H A Haenssle, et al.
International Journal of Surgery Case Reports|June 28, 2021
Prognostic assessment and management of a patient with Carmi syndrome. A case reportD Schreiner, A Uebler, C Ginghina, et al.
Skin Health and Disease|June 6, 2022
Rothmund-Thomson syndrome type 1 caused by biallelic ANAPC1 gene mutationsB Zirn, U Bernbeck, K Alt, et al.
The British Journal of Dermatology|October 20, 2018
Alitretinoin in punctate palmoplantar keratodermaP Yilmaz, M Medvecz, J Kohlhase, et al.
The British Journal of Dermatology|October 29, 2014
Blaschko line acne on pre-existent hypomelanosis reflecting a mosaic FGFR2 mutationD Kiritsi, A I Lorente, R Happle, et al.
The British Journal of Dermatology|July 22, 2014
Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergiesC Has, T Jakob, Y He, et al.
The British Journal of Dermatology|March 1, 2019
Extending the phenotypic spectrum associated with mosaicism for GJB2 mutationsC Has, J Küsel, R Happle, et al.
Pageof 9

Showing results (31-40 of 90) with videos related to

Sort By:
Pageof 9
Journal of Cellular and Molecular Medicine|June 18, 2002
Genetic analysis of factor V Leiden in a family with history of thrombosis and venous leg ulcersLucia M. Procopciuc, C. Has, C. Drugan, et al.
The British Journal of Dermatology|September 21, 2011
Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutationB Burger, I Spoerri, M Schubert, et al.
Annales De Dermatologie Et De Venereologie|January 29, 1999
[Multiple cutaneous cylindromas associated with parotid and submandibular gland cylindromas]A Baican, C Has, C Crisan, et al.
Clinical and Experimental Dermatology|June 11, 2013
Epidermolysis bullosa simplex: greater penetrance due to a keratin 5 gene variantM Jantke, C Has, H A Haenssle, et al.
International Journal of Surgery Case Reports|June 28, 2021
Prognostic assessment and management of a patient with Carmi syndrome. A case reportD Schreiner, A Uebler, C Ginghina, et al.
Skin Health and Disease|June 6, 2022
Rothmund-Thomson syndrome type 1 caused by biallelic ANAPC1 gene mutationsB Zirn, U Bernbeck, K Alt, et al.
The British Journal of Dermatology|October 20, 2018
Alitretinoin in punctate palmoplantar keratodermaP Yilmaz, M Medvecz, J Kohlhase, et al.
The British Journal of Dermatology|October 29, 2014
Blaschko line acne on pre-existent hypomelanosis reflecting a mosaic FGFR2 mutationD Kiritsi, A I Lorente, R Happle, et al.
The British Journal of Dermatology|July 22, 2014
Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergiesC Has, T Jakob, Y He, et al.
The British Journal of Dermatology|March 1, 2019
Extending the phenotypic spectrum associated with mosaicism for GJB2 mutationsC Has, J Küsel, R Happle, et al.
Pageof 9