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Proteins|January 12, 2008
Role of the amino acid sequence in domain swapping of the B1 domain of protein GFernanda L Sirota, Stephanie Héry-Huynh, Sebastian Maurer-Stroh, et al.Prenatal Diagnosis|December 13, 2000
Prenatal diagnosis of a novel COL1A1 mutation in osteogenesis imperfecta type I carried through full term pregnancyL Ries, M Frydman, G Barkai, et al.The Journal of Trauma|March 1, 1996
Computed tomography detection of active mesenteric hemorrhage following blunt abdominal traumaR Sher, G M Frydman, T J Russell, et al.Helvetica Paediatrica Acta|December 1, 1984
Myocarditis and acute infantile hemiparesis. Case reportA Ashkenazi, M Frydman, R Weitz, et al.European Journal of Pediatrics|August 1, 1989
Cardiac involvement in glycogen storage disease type IIIS W Moses, K L Wanderman, A Myroz, et al.Clinical Genetics|August 1, 1990
Megalocornea, macrocephaly, mental and motor retardation (MMMM)M Frydman, M Berkenstadt, A Raas-Rothschild, et al.Genetic Epidemiology|January 1, 1986
Evidence for linkage between Wilson disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study methodB Bonné-Tamir, L A Farrer, M Frydman, et al.Journal of Pediatric Gastroenterology and Nutrition|August 1, 1991
Childhood protein-losing enteropathy associated with Helicobacter pylori infectionH A Cohen, R P Shapiro, M Frydman, et al.Journal of Medical Genetics|June 1, 1979
Triple mosaicism 45,XY,--18/46, XY/47,XY,+18M Frydman, F Shabtai, Y Barak, et al.Harefuah|June 15, 1995
[Multidisciplinary approach to counseling in Huntington's disease]N Dangoor, E Gazit, M Sade, et al.Pageof 35