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American Journal of Ophthalmology|June 1, 1996
Diagnosis of oculocutaneous albinism with molecular analysisC G Summers, W S Oetting, R A KingHuman Heredity|October 3, 2009
Pair-wise multifactor dimensionality reduction method to detect gene-gene interactions in a case-control studyH He, W S Oetting, M J Brott, et al.Pigment Cell Research|June 1, 1993
Evolution of the tyrosinase related gene (TYRL) in primatesW S Oetting, O C Stine, D Townsend, et al.The Journal of Experimental Zoology|August 1, 1985
C pigment locus mutants of the fowl produce enzymatically inactive tyrosinase-like moleculesW S Oetting, A M Churilla, H Yamamoto, et al.The Journal of Investigative Dermatology|November 17, 2001
Alternative splicing of the tyrosinase gene transcript in normal human melanocytes and lymphocytesJ P Fryer, W S Oetting, M J Brott, 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.Pageof 36