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S J Bale

Showing results (51-60 of 99) with videos related to

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Nature Genetics|December 1, 1995
Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevusG Richard, V De Laurenzi, B Didona, et al.
American Journal of Human Genetics|May 1, 1994
Localization of the gene for the nevoid basal cell carcinoma syndromeA M Goldstein, C Stewart, A E Bale, et al.
American Journal of Human Genetics|December 1, 1994
Linkage of autosomal recessive lamellar ichthyosis to chromosome 14qL J Russell, J J DiGiovanna, N Hashem, et al.
Human Genetics|July 29, 2000
Splice-site mutation in TGM1 in congenital recessive ichthyosis in American families: molecular, genetic, genealogic, and clinical studiesY O Shevchenko, J G Compton, J R Toro, et al.
The Journal of Investigative Dermatology|December 1, 1996
Congenital recessive ichthyosis unlinked to loci for epidermal transglutaminasesS J Bale, L J Russell, M L Lee, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndromeA E Bale, S J Bale, H Murli, et al.
International Journal of Cancer|October 15, 1985
Hereditary malignant melanoma is not linked to the HLA complex on chromosome 6S J Bale, M H Greene, C Murray, et al.
Journal of Medical Genetics|September 1, 1987
Genetic linkage studies with neurofibromatosis: the question of heterogeneityM A Spence, R S Sparkes, D M Parry, et al.
The Journal of Investigative Dermatology|December 1, 1994
A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratodermaV Kimonis, J J DiGiovanna, J M Yang, et al.
American Journal of Human Genetics|November 1, 1995
Genetic homogeneity in Sjögren-Larsson syndrome: linkage to chromosome 17p in families of different non-Swedish ethnic originsG R Rogers, W B Rizzo, A Zlotogorski, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Nature Genetics|December 1, 1995
Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevusG Richard, V De Laurenzi, B Didona, et al.
American Journal of Human Genetics|May 1, 1994
Localization of the gene for the nevoid basal cell carcinoma syndromeA M Goldstein, C Stewart, A E Bale, et al.
American Journal of Human Genetics|December 1, 1994
Linkage of autosomal recessive lamellar ichthyosis to chromosome 14qL J Russell, J J DiGiovanna, N Hashem, et al.
Human Genetics|July 29, 2000
Splice-site mutation in TGM1 in congenital recessive ichthyosis in American families: molecular, genetic, genealogic, and clinical studiesY O Shevchenko, J G Compton, J R Toro, et al.
The Journal of Investigative Dermatology|December 1, 1996
Congenital recessive ichthyosis unlinked to loci for epidermal transglutaminasesS J Bale, L J Russell, M L Lee, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndromeA E Bale, S J Bale, H Murli, et al.
International Journal of Cancer|October 15, 1985
Hereditary malignant melanoma is not linked to the HLA complex on chromosome 6S J Bale, M H Greene, C Murray, et al.
Journal of Medical Genetics|September 1, 1987
Genetic linkage studies with neurofibromatosis: the question of heterogeneityM A Spence, R S Sparkes, D M Parry, et al.
The Journal of Investigative Dermatology|December 1, 1994
A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratodermaV Kimonis, J J DiGiovanna, J M Yang, et al.
American Journal of Human Genetics|November 1, 1995
Genetic homogeneity in Sjögren-Larsson syndrome: linkage to chromosome 17p in families of different non-Swedish ethnic originsG R Rogers, W B Rizzo, A Zlotogorski, et al.
Pageof 10