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Human Genetics|July 8, 1999
Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndromeL R Cornejo-Roldan, E Roessler, M MuenkeEuropean Journal of Pharmacology|March 26, 1981
Relative activities of substances related to 5-hydroxytryptamine as depolarizing agents of superior cervical ganglion cellsD Wallis, H NashAmerican Journal of Medical Genetics|March 15, 1996
Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toesN H Robin, B Segel, G Carpenter, et al.Genomics|January 1, 1993
Regional assignment of the human homeobox-containing gene EN1 to chromosome 2q13-q21A Köhler, C Logan, A L Joyner, et al.Acta Crystallographica. Section E, Crystallographic Communications|January 11, 2023
Crystal structure of bis-(mesit-yl)(pyrrol-1-yl)boraneOnur Sahin, John D WallisOrganic & Biomolecular Chemistry|December 26, 2008
Interactions and reactions in some 2,2'-disubstituted biphenyls--an open or shut caseJane O'Leary, John D WallisMolecular Genetics and Metabolism|July 31, 1998
Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4K Gaudenz, E Roessler, S Vainikka, et al.The Journal of Heredity|November 1, 1994
Mapping the bovine homolog of the human cystic fibrosis geneD Wallis, J E WomackChemistry (Weinheim an Der Bergstrasse, Germany)|July 21, 2006
Weak attractive interactions between methylthio groups and electron-deficient alkenes in peri-naphthalenes: a competition with conjugative effectsJane O'Leary, John D WallisArchives of Disease in Childhood|March 29, 2002
Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephalyH S Heussler, M Suri, I D Young, et al.Pageof 49