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H P Stevens

Showing results (51-60 of 57) with videos related to

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The British Journal of Dermatology|February 26, 2009
Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi populationC Sinclair, E A O'Toole, D Paige, et al.
Human Molecular Genetics|June 1, 1996
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC)D P Kelsell, J M Risk, I M Leigh, et al.
Human Molecular Genetics|May 20, 1999
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.
Techniques in Coloproctology|October 4, 2021
Efficacy and safety of autologous adipose-derived stromal vascular fraction enriched with platelet-rich plasma in flap repair of transsphincteric cryptoglandular fistulasW R Schouten, J H C Arkenbosch, C J van der Woude, et al.
Genomics|July 20, 1999
Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25J M Risk, C Ruhrberg, H Hennies, et al.
American Journal of Human Genetics|July 27, 1999
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencingM van Steensel, F J Smith, P M Steijlen, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratodermaD M Hunt, L Rickman, N V Whittock, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
The British Journal of Dermatology|February 26, 2009
Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi populationC Sinclair, E A O'Toole, D Paige, et al.
Human Molecular Genetics|June 1, 1996
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC)D P Kelsell, J M Risk, I M Leigh, et al.
Human Molecular Genetics|May 20, 1999
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.
Techniques in Coloproctology|October 4, 2021
Efficacy and safety of autologous adipose-derived stromal vascular fraction enriched with platelet-rich plasma in flap repair of transsphincteric cryptoglandular fistulasW R Schouten, J H C Arkenbosch, C J van der Woude, et al.
Genomics|July 20, 1999
Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25J M Risk, C Ruhrberg, H Hennies, et al.
American Journal of Human Genetics|July 27, 1999
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencingM van Steensel, F J Smith, P M Steijlen, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratodermaD M Hunt, L Rickman, N V Whittock, et al.
Pageof 6