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Journal of Biophotonics|July 26, 2023
Raman spectroscopy for postmortem interval estimation of human skeletal remains: A scoping reviewC Woess, Christian W Huck, J Badzoka, et al.Human Molecular Genetics|February 1, 1995
Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyS Kosugi, C Van Dop, M E Geffner, et al.Science (New York, N.Y.)|April 21, 1995
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 24, 2012
Diabetes mellitus in children and adolescents with genetic syndromesF Schmidt, T M Kapellen, S Wiegand, et al.Human Mutation|June 30, 2000
The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight familiesT Raz, V Labay, D Baron, et al.The Journal of Clinical Endocrinology and Metabolism|October 14, 2011
Three-year growth hormone treatment in short children with X-linked hypophosphatemic rickets: effects on linear growth and body disproportionM Živičnjak, D Schnabel, H Staude, et al.The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Evaluation of gonadal function in 107 intersex patients by means of serum antimüllerian hormone measurementR A Rey, C Belville, C Nihoul-Fékété, et al.Pageof 9