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Y de Prost

Showing results (131-140 of 181) with videos related to

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The Journal of Pathology|March 1, 1997
Lack of expression of E-cadherin is associated with dissemination of Langerhans' cell histiocytosis and poor outcomeF Geissmann, J F Emile, P Andry, et al.
Annales De Dermatologie Et De Venereologie|December 4, 1998
[Skin manifestations of protein glycosylation deficiency, the CDG (carbohydrate deficient glycoprotein) type 1 syndrome]P Vabres, C Sevin, J C Amoric, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1995
[Cutaneous transformation of chronic lymphoid leukemia into immunoblastic lymphoma. Cutaneous manifestation of Richter syndrome]S Fraitag, C Bodemer, P Rousselot, et al.
American Journal of Human Genetics|August 1, 1994
Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosaA Hovnanian, L Hilal, C Blanchet-Bardon, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1993
[Early surgical treatment of eyelid angioma]S Cabut, D Teillac-Hamel, P Delanoe, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysisP Lefevre, A Rochat, C Bodemer, et al.
Annales De Dermatologie Et De Venereologie|August 10, 2000
[Rothmund-Thomson syndrome and defective DNA excision-resynthesis repair]N Bodak, C Bodemer, A Sarasin, et al.
The British Journal of Dermatology|July 1, 1994
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 casesC Bodemer, Y De Prost, B Bachollet, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1985
[Generalized diabetic lipoatrophy in children]M F Galezowski, M M Lanza, R Brauner, et al.
Human Molecular Genetics|November 2, 2001
Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with agingY Gache, M Allegra, C Bodemer, et al.
Pageof 19

Showing results (131-140 of 181) with videos related to

Sort By:
Pageof 19
The Journal of Pathology|March 1, 1997
Lack of expression of E-cadherin is associated with dissemination of Langerhans' cell histiocytosis and poor outcomeF Geissmann, J F Emile, P Andry, et al.
Annales De Dermatologie Et De Venereologie|December 4, 1998
[Skin manifestations of protein glycosylation deficiency, the CDG (carbohydrate deficient glycoprotein) type 1 syndrome]P Vabres, C Sevin, J C Amoric, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1995
[Cutaneous transformation of chronic lymphoid leukemia into immunoblastic lymphoma. Cutaneous manifestation of Richter syndrome]S Fraitag, C Bodemer, P Rousselot, et al.
American Journal of Human Genetics|August 1, 1994
Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosaA Hovnanian, L Hilal, C Blanchet-Bardon, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1993
[Early surgical treatment of eyelid angioma]S Cabut, D Teillac-Hamel, P Delanoe, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysisP Lefevre, A Rochat, C Bodemer, et al.
Annales De Dermatologie Et De Venereologie|August 10, 2000
[Rothmund-Thomson syndrome and defective DNA excision-resynthesis repair]N Bodak, C Bodemer, A Sarasin, et al.
The British Journal of Dermatology|July 1, 1994
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 casesC Bodemer, Y De Prost, B Bachollet, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1985
[Generalized diabetic lipoatrophy in children]M F Galezowski, M M Lanza, R Brauner, et al.
Human Molecular Genetics|November 2, 2001
Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with agingY Gache, M Allegra, C Bodemer, et al.
Pageof 19