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O Dereure

Showing results (111-120 of 288) with videos related to

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Annales De Dermatologie Et De Venereologie|April 19, 2011
[Mutations of C16orf57 gene have been identified in the poikiloderma-neutropenia syndrome and in a specific subset of congenital dyskeratosis with normal-length telomeres]O Dereure
Annales De Dermatologie Et De Venereologie|December 8, 2010
[Peeling skin disease: the responsibility of corneodesmosin]O Dereure
Annales De Dermatologie Et De Venereologie|November 15, 2011
[Multiple self-healing squamous epithelioma, or Ferguson-Smith disease: demonstration of mutations in the TGFβ-receptor]O Dereure
Annales De Dermatologie Et De Venereologie|January 10, 2012
[Adermatoglyphia or "immigration delay disease": the role of mutations in the SMARCAD1 gene]O Dereure
Annales De Dermatologie Et De Venereologie|September 7, 2011
[Psoriasis: new susceptibility loci]O Dereure
Annales De Dermatologie Et De Venereologie|July 6, 2004
[Mutation of the fibulin-5 gene in recessive autosomal cutis laxa]O Dereure
Annales De Dermatologie Et De Venereologie|March 26, 2004
[Hopf's verruciform acrokeratosis and Darier's disease are related to mutations in the same gene, ATP2A2]O Dereure
Annales De Dermatologie Et De Venereologie|April 27, 2004
[Autoregressive sealy baby: mutations in transglutaminase 1 with varying effects]O Dereure
Annales De Dermatologie Et De Venereologie|October 19, 2005
[Hartnup disease is related to a mutation in the SL C6A19 gene coding for the B degrees AT1 aminoacid transporter]O Dereure
Annales De Dermatologie Et De Venereologie|November 18, 2009
[Differentiating between Mednik and Cednik syndromes]O Dereure
Pageof 29

Showing results (111-120 of 288) with videos related to

Sort By:
Pageof 29
Annales De Dermatologie Et De Venereologie|April 19, 2011
[Mutations of C16orf57 gene have been identified in the poikiloderma-neutropenia syndrome and in a specific subset of congenital dyskeratosis with normal-length telomeres]O Dereure
Annales De Dermatologie Et De Venereologie|December 8, 2010
[Peeling skin disease: the responsibility of corneodesmosin]O Dereure
Annales De Dermatologie Et De Venereologie|November 15, 2011
[Multiple self-healing squamous epithelioma, or Ferguson-Smith disease: demonstration of mutations in the TGFβ-receptor]O Dereure
Annales De Dermatologie Et De Venereologie|January 10, 2012
[Adermatoglyphia or "immigration delay disease": the role of mutations in the SMARCAD1 gene]O Dereure
Annales De Dermatologie Et De Venereologie|September 7, 2011
[Psoriasis: new susceptibility loci]O Dereure
Annales De Dermatologie Et De Venereologie|July 6, 2004
[Mutation of the fibulin-5 gene in recessive autosomal cutis laxa]O Dereure
Annales De Dermatologie Et De Venereologie|March 26, 2004
[Hopf's verruciform acrokeratosis and Darier's disease are related to mutations in the same gene, ATP2A2]O Dereure
Annales De Dermatologie Et De Venereologie|April 27, 2004
[Autoregressive sealy baby: mutations in transglutaminase 1 with varying effects]O Dereure
Annales De Dermatologie Et De Venereologie|October 19, 2005
[Hartnup disease is related to a mutation in the SL C6A19 gene coding for the B degrees AT1 aminoacid transporter]O Dereure
Annales De Dermatologie Et De Venereologie|November 18, 2009
[Differentiating between Mednik and Cednik syndromes]O Dereure
Pageof 29