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H P Stevens

Showing results (41-50 of 57) with videos related to

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Nature|May 1, 1997
Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessD P Kelsell, J Dunlop, H P Stevens, et al.
The British Journal of Dermatology|January 20, 1999
Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stressO Swensson, L Langbein, J R McMillan, et al.
Nature Genetics|August 1, 1997
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrixH Winter, M A Rogers, L Langbein, et al.
Human Genetics|December 24, 1997
A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrixH Winter, M A Rogers, M Gebhardt, et al.
Archives of Dermatology|June 1, 1996
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermasH P Stevens, D P Kelsell, S P Bryant, et al.
Journal of Hand Surgery (Edinburgh, Scotland)|December 1, 1992
Replantation of the radial side of the hand in the rhesus monkey: anatomical and functional aspects. A preliminary study to composite tissue allograftingS E Hovius, H P Stevens, P W Van Nierop, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 30, 1999
Symmetry and morbidity assessment of unilateral complete cleft lip nose corrected with or without primary nasal correctionC A Brussé, J F Van der Werff, H P Stevens, et al.
The Journal of Investigative Dermatology|May 1, 1995
Characterization of paraneoplastic pemphigus autoantigens by immunoblot analysisT Hashimoto, M Amagai, K Watanabe, et al.
Human Molecular Genetics|November 7, 2000
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratodermaE E Norgett, S J Hatsell, L Carvajal-Huerta, et al.
Human Molecular Genetics|October 1, 1995
Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two familiesM K Shamsher, H A Navsaria, H P Stevens, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Nature|May 1, 1997
Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessD P Kelsell, J Dunlop, H P Stevens, et al.
The British Journal of Dermatology|January 20, 1999
Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stressO Swensson, L Langbein, J R McMillan, et al.
Nature Genetics|August 1, 1997
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrixH Winter, M A Rogers, L Langbein, et al.
Human Genetics|December 24, 1997
A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrixH Winter, M A Rogers, M Gebhardt, et al.
Archives of Dermatology|June 1, 1996
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermasH P Stevens, D P Kelsell, S P Bryant, et al.
Journal of Hand Surgery (Edinburgh, Scotland)|December 1, 1992
Replantation of the radial side of the hand in the rhesus monkey: anatomical and functional aspects. A preliminary study to composite tissue allograftingS E Hovius, H P Stevens, P W Van Nierop, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 30, 1999
Symmetry and morbidity assessment of unilateral complete cleft lip nose corrected with or without primary nasal correctionC A Brussé, J F Van der Werff, H P Stevens, et al.
The Journal of Investigative Dermatology|May 1, 1995
Characterization of paraneoplastic pemphigus autoantigens by immunoblot analysisT Hashimoto, M Amagai, K Watanabe, et al.
Human Molecular Genetics|November 7, 2000
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratodermaE E Norgett, S J Hatsell, L Carvajal-Huerta, et al.
Human Molecular Genetics|October 1, 1995
Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two familiesM K Shamsher, H A Navsaria, H P Stevens, et al.
Pageof 6