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W S Oetting

Showing results (31-40 of 54) with videos related to

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Nucleic Acids Research|October 25, 1991
PCR detection of a TaqI polymorphism at the CCAATT box of the human tyrosinase (TYR) geneW S Oetting, C M Roed, M M Mentink, et al.
Clinical Genetics|May 4, 2011
Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screeningK Sarafoglou, C P Lorentz, N Otten, et al.
Ophthalmic Genetics|January 3, 2001
Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN)W S Oetting, C M Armstrong, A M Holleschau, et al.
American Journal of Human Genetics|October 1, 1995
A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2S C Wildenberg, W S Oetting, C Almodóvar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2001
Molecular analysis of an extended Palestinian family from Israel with monilethrixW S Oetting, J P Fryer, Z Wyman, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 6, 2012
Lower calcineurin inhibitor doses in older compared to younger kidney transplant recipients yield similar troughsP A Jacobson, D Schladt, W S Oetting, et al.
The Journal of Investigative Dermatology|May 14, 1998
Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto RicoS C Wildenberg, J P Fryer, J M Gardner, et al.
The Journal of Investigative Dermatology|July 1, 1991
Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinismW S Oetting, H Y Handoko, M M Mentink, et al.
Electrophoresis|February 5, 1999
Multiplexed short tandem repeat polymorphisms of the Weber 8A set of markers using tailed primers and infrared fluorescence detectionW S Oetting, C M Armstrong, S M Ronan, et al.
American Journal of Human Genetics|July 1, 1991
Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinismW S Oetting, M M Mentink, C G Summers, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Nucleic Acids Research|October 25, 1991
PCR detection of a TaqI polymorphism at the CCAATT box of the human tyrosinase (TYR) geneW S Oetting, C M Roed, M M Mentink, et al.
Clinical Genetics|May 4, 2011
Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screeningK Sarafoglou, C P Lorentz, N Otten, et al.
Ophthalmic Genetics|January 3, 2001
Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN)W S Oetting, C M Armstrong, A M Holleschau, et al.
American Journal of Human Genetics|October 1, 1995
A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2S C Wildenberg, W S Oetting, C Almodóvar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2001
Molecular analysis of an extended Palestinian family from Israel with monilethrixW S Oetting, J P Fryer, Z Wyman, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 6, 2012
Lower calcineurin inhibitor doses in older compared to younger kidney transplant recipients yield similar troughsP A Jacobson, D Schladt, W S Oetting, et al.
The Journal of Investigative Dermatology|May 14, 1998
Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto RicoS C Wildenberg, J P Fryer, J M Gardner, et al.
The Journal of Investigative Dermatology|July 1, 1991
Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinismW S Oetting, H Y Handoko, M M Mentink, et al.
Electrophoresis|February 5, 1999
Multiplexed short tandem repeat polymorphisms of the Weber 8A set of markers using tailed primers and infrared fluorescence detectionW S Oetting, C M Armstrong, S M Ronan, et al.
American Journal of Human Genetics|July 1, 1991
Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinismW S Oetting, M M Mentink, C G Summers, et al.
Pageof 6