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W S Oetting

Showing results (41-50 of 54) with videos related to

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Genomics|December 10, 1995
Linkage analysis with multiplexed short tandem repeat polymorphisms using infrared fluorescence and M13 tailed primersW S Oetting, H K Lee, D J Flanders, et al.
American Journal of Human Genetics|January 1, 1993
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto RicoW S Oetting, C J Witkop, S A Brown, et al.
Human Mutation|February 12, 2000
Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. OnlineW S Oetting, J M Gardner, J P Fryer, et al.
Electrophoresis|February 1, 1994
Analysis of tyrosinase gene mutations using direct automated infrared fluorescence DNA sequencing of amplified exonsW S Oetting, J P Fryer, Y Oofuji, et al.
Pigment Cell Research|July 1, 1999
Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluationR K Tripathi, D J Flanders, T L Young, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 18, 2000
BRCA1 susceptibility markers and postmenopausal breast cancer: the Iowa Women's Health StudyJ A Thompson, P L Chen, R A King, et al.
American Journal of Human Genetics|October 30, 1998
A second locus for familial high myopia maps to chromosome 12qT L Young, S M Ronan, A B Alvear, et al.
The Pharmacogenomics Journal|November 22, 2017
Genome-wide association study identifies the common variants in CYP3A4 and CYP3A5 responsible for variation in tacrolimus trough concentration in Caucasian kidney transplant recipientsW S Oetting, B Wu, D P Schladt, et al.
American Journal of Human Genetics|June 23, 1998
Evidence that a locus for familial high myopia maps to chromosome 18pT L Young, S M Ronan, L A Drahozal, et al.
American Journal of Human Genetics|June 1, 1996
Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3"R E Boissy, H Zhao, W S Oetting, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Genomics|December 10, 1995
Linkage analysis with multiplexed short tandem repeat polymorphisms using infrared fluorescence and M13 tailed primersW S Oetting, H K Lee, D J Flanders, et al.
American Journal of Human Genetics|January 1, 1993
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto RicoW S Oetting, C J Witkop, S A Brown, et al.
Human Mutation|February 12, 2000
Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. OnlineW S Oetting, J M Gardner, J P Fryer, et al.
Electrophoresis|February 1, 1994
Analysis of tyrosinase gene mutations using direct automated infrared fluorescence DNA sequencing of amplified exonsW S Oetting, J P Fryer, Y Oofuji, et al.
Pigment Cell Research|July 1, 1999
Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluationR K Tripathi, D J Flanders, T L Young, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 18, 2000
BRCA1 susceptibility markers and postmenopausal breast cancer: the Iowa Women's Health StudyJ A Thompson, P L Chen, R A King, et al.
American Journal of Human Genetics|October 30, 1998
A second locus for familial high myopia maps to chromosome 12qT L Young, S M Ronan, A B Alvear, et al.
The Pharmacogenomics Journal|November 22, 2017
Genome-wide association study identifies the common variants in CYP3A4 and CYP3A5 responsible for variation in tacrolimus trough concentration in Caucasian kidney transplant recipientsW S Oetting, B Wu, D P Schladt, et al.
American Journal of Human Genetics|June 23, 1998
Evidence that a locus for familial high myopia maps to chromosome 18pT L Young, S M Ronan, L A Drahozal, et al.
American Journal of Human Genetics|June 1, 1996
Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3"R E Boissy, H Zhao, W S Oetting, et al.
Pageof 6