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Journal of Medical Genetics|December 1, 1986
Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyV M Kean, H L Macleod, M W Thompson, et al.Case Reports in Pediatrics|December 4, 2020
Altered Mental Status and Cyanosis in a Pediatric Patient with MethemoglobinemiaPhillip M Grenz, Robert N Ray, Olivia A Hardy, et al.Applied Optics|December 28, 2020
Mechanisms influencing and prediction of tool influence function spots during hemispherical sub-aperture tool polishing on fused silicaT Suratwala, J Menapace, R Steele, et al.Academic Pediatrics|March 20, 2021
Antibiotic Prescribing for Acute Respiratory Tract Infections During Telemedicine Visits Within a Pediatric Primary Care NetworkKristin N Ray, Judith M Martin, David Wolfson, et al.Journal of Medical Genetics|June 1, 1988
Partial gene duplication in Duchenne and Becker muscular dystrophiesX Y Hu, A H Burghes, P N Ray, et al.Science (New York, N.Y.)|September 25, 1987
Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophyS E Bodrug, P N Ray, I L Gonzalez, et al.Journal of Medical Genetics|July 1, 1990
Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophyS E Bodrug, J R Roberson, L Weiss, et al.Genes & Development|November 17, 2012
The SMAD2/3 corepressor SNON maintains pluripotency through selective repression of mesendodermal genes in human ES cellsNorihiro Tsuneyoshi, Ee Kim Tan, Akila Sadasivam, et al.Molecular Endocrinology (Baltimore, Md.)|May 10, 2012
Research resource: identification of novel growth hormone-regulated phosphorylation sites by quantitative phosphoproteomicsBridgette N Ray, Hye Kyong Kweon, Lawrence S Argetsinger, et al.Studies in Health Technology and Informatics|September 14, 2004
Impact of patient feedback on residents' handheld computer use: a multi-site studyEta S Berner, Grant T Savage, Thomas K Houston, et al.Pageof 56