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S J Bale

Showing results (81-90 of 99) with videos related to

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Nature|January 1, 1987
Evidence against Ha-ras-1 involvement in sporadic and familial melanomaD S Gerhard, N C Dracopoli, S J Bale, et al.
Genomics|August 1, 1988
Two thyroid hormone regulated genes, the beta-subunits of nerve growth factor (NGFB) and thyroid stimulating hormone (TSHB), are located less than 310 kb apart in both human and mouse genomesN C Dracopoli, E Rose, G K Whitfield, et al.
Carcinogenesis|October 7, 2000
A new xeroderma pigmentosum group C poly(AT) insertion/deletion polymorphismS G Khan, E J Metter, R E Tarone, et al.
Nature Genetics|December 8, 1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilisG Richard, L E Smith, R A Bailey, et al.
Genomics|April 1, 1989
Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11S J Bale, A E Bale, K Stewart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Genealogy construction in a historically isolated population: application to genetic studies of rheumatoid arthritis in the Pima IndianJ P Lin, R Hirsch, L T Jacobsson, et al.
The Journal of Investigative Dermatology|July 1, 1997
Sjögren-Larsson syndrome is caused by a common mutation in northern European and Swedish patientsV De Laurenzi, G R Rogers, E Tarcsa, et al.
Cell|April 3, 1992
Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9M R Gailani, S J Bale, D J Leffell, et al.
American Journal of Human Genetics|March 1, 1993
Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneityA M Goldstein, N C Dracopoli, E C Ho, et al.
The Journal of Investigative Dermatology|November 5, 1997
Linkage studies in erythrokeratodermias: fine mapping, genetic heterogeneity and analysis of candidate genesG Richard, J P Lin, L Smith, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Nature|January 1, 1987
Evidence against Ha-ras-1 involvement in sporadic and familial melanomaD S Gerhard, N C Dracopoli, S J Bale, et al.
Genomics|August 1, 1988
Two thyroid hormone regulated genes, the beta-subunits of nerve growth factor (NGFB) and thyroid stimulating hormone (TSHB), are located less than 310 kb apart in both human and mouse genomesN C Dracopoli, E Rose, G K Whitfield, et al.
Carcinogenesis|October 7, 2000
A new xeroderma pigmentosum group C poly(AT) insertion/deletion polymorphismS G Khan, E J Metter, R E Tarone, et al.
Nature Genetics|December 8, 1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilisG Richard, L E Smith, R A Bailey, et al.
Genomics|April 1, 1989
Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11S J Bale, A E Bale, K Stewart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Genealogy construction in a historically isolated population: application to genetic studies of rheumatoid arthritis in the Pima IndianJ P Lin, R Hirsch, L T Jacobsson, et al.
The Journal of Investigative Dermatology|July 1, 1997
Sjögren-Larsson syndrome is caused by a common mutation in northern European and Swedish patientsV De Laurenzi, G R Rogers, E Tarcsa, et al.
Cell|April 3, 1992
Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9M R Gailani, S J Bale, D J Leffell, et al.
American Journal of Human Genetics|March 1, 1993
Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneityA M Goldstein, N C Dracopoli, E C Ho, et al.
The Journal of Investigative Dermatology|November 5, 1997
Linkage studies in erythrokeratodermias: fine mapping, genetic heterogeneity and analysis of candidate genesG Richard, J P Lin, L Smith, et al.
Pageof 10