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R S Bladergroen

Showing results (1-10 of 8) with videos related to

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Bio Systems|September 27, 2000
Computing with DNA by operating on plasmidsT Head, G Rozenberg, R S Bladergroen, et al.
Journal of Medical Genetics|March 4, 2005
A missense mutation in the type II hair keratin hHb3 is associated with monilethrixM A M van Steensel, P M Steijlen, R S Bladergroen, et al.
The British Journal of Dermatology|May 27, 2010
A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosisM C Bolling, R S Bladergroen, M A M van Steensel, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratodermaM A M van Steensel, L Spruijt, I van der Burgt, et al.
Human Mutation|September 18, 2009
Novel missense mutations in the FOXC2 gene alter transcriptional activityM A M van Steensel, R J Damstra, M V Heitink, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Exclusion of ferrochelatase gene mutations in patients with seasonal palmoplantar keratodermaR J Schimmel, A M Van Tuyll Van Serooskerke, R S Bladergroen, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Identification of a recurrent mutation in the protoporphyrinogen oxidase gene in Swiss patients with variegate porphyria: clinical and genetic implicationsA M Van Tuyll Van Serooskerke, X Schneider-Yin, R J Schimmel, et al.
The British Journal of Dermatology|September 14, 2011
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestryA M van Tuyll van Serooskerken, B I Drögemöller, K Te Velde, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Bio Systems|September 27, 2000
Computing with DNA by operating on plasmidsT Head, G Rozenberg, R S Bladergroen, et al.
Journal of Medical Genetics|March 4, 2005
A missense mutation in the type II hair keratin hHb3 is associated with monilethrixM A M van Steensel, P M Steijlen, R S Bladergroen, et al.
The British Journal of Dermatology|May 27, 2010
A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosisM C Bolling, R S Bladergroen, M A M van Steensel, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratodermaM A M van Steensel, L Spruijt, I van der Burgt, et al.
Human Mutation|September 18, 2009
Novel missense mutations in the FOXC2 gene alter transcriptional activityM A M van Steensel, R J Damstra, M V Heitink, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Exclusion of ferrochelatase gene mutations in patients with seasonal palmoplantar keratodermaR J Schimmel, A M Van Tuyll Van Serooskerke, R S Bladergroen, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Identification of a recurrent mutation in the protoporphyrinogen oxidase gene in Swiss patients with variegate porphyria: clinical and genetic implicationsA M Van Tuyll Van Serooskerke, X Schneider-Yin, R J Schimmel, et al.
The British Journal of Dermatology|September 14, 2011
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestryA M van Tuyll van Serooskerken, B I Drögemöller, K Te Velde, et al.
Pageof 1