Showing results (291-300 of 999) with videos related to
Sort By:
Pageof 100
Human Mutation|January 1, 1994
Two NF1 mutations: frameshift in the GAP-related domain, and loss of two codons toward the 3' end of the geneC R Abernathy, S D Colman, B G Kousseff, et al.Acta Haematologica|January 1, 1984
Hemorrhagic diathesis in multiple myelomaM R Wallace, S R Simon, W B Ershler, et al.Genomics|June 1, 1990
Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3S A Ledbetter, M R Wallace, F S Collins, et al.American Journal of Medical Genetics|October 1, 1986
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American familyM R Wallace, P M Conneally, G L Long, et al.Clinical Endocrinology|November 6, 2012
Sex hormone binding globulin and insulin resistanceIan R Wallace, Michelle C McKinley, Patrick M Bell, et al.The Pharmacogenomics Journal|December 7, 2019
OPRM1, OPRK1, and COMT genetic polymorphisms associated with opioid effects on experimental pain: a randomized, double-blind, placebo-controlled studyKwo Wei David Ho, Margaret R Wallace, Roland Staud, et al.Veterinary Ophthalmology|May 25, 2005
Inheritance of cataract in the Bichon FriseM R Wallace, E O MacKay, K N Gelatt, et al.Genetic Testing|January 11, 2000
Elastin region deletions in Williams syndromeJ Zhang, A Kumar, K Roux, et al.Journal of Animal Science|August 1, 1984
A review of endocrine regulation of metabolism during lactationR J Collier, J P McNamara, C R Wallace, et al.Journal of Medical Genetics|July 1, 1997
Four frameshift mutations in neurofibromatosis type 1 caused by small insertionsS D Colman, C R Abernathy, V T Ho, et al.Pageof 100