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The British Journal of Psychiatry : the Journal of Mental Science|September 1, 1988
Post-partum psychosis in adult GM2 gangliosidosis. A case reportP Lichtenberg, R Navon, E Wertman, et al.Journal of Medical Genetics|June 1, 1983
Intestinal obstruction and cystic fibrosis: antenatal ultrasound appearanceJ Shalev, R Navon, D Urbach, et al.Prenatal Diagnosis|May 1, 1986
Adult-onset GM2 gangliosidosis diagnosed in a fetusR Navon, U Sandbank, A Frisch, et al.Molecular Genetics and Metabolism|April 6, 2010
Two novel exonic point mutations in HEXA identified in a juvenile Tay-Sachs patient: role of alternative splicing and nonsense-mediated mRNA decayA Levit, D Nutman, E Osher, et al.Journal of Child Neurology|June 8, 2001
31Phosphorus magnetic resonance spectroscopy in late-onset Tay-Sachs diseaseU Felderhoff-Mueser, J Sperner, P Konstanzcak, et al.Human Mutation|January 1, 1997
Molecular basis of heat labile hexosaminidase B among Jews and ArabsG Narkis, A Adam, L Jaber, et al.Israel Journal of Medical Sciences|December 1, 1976
Tay-Sachs disease in a Moroccan Jewish family: a possible new mutationG Bach, R Navon, M Zeigler, et al.American Journal of Human Genetics|April 1, 1990
Ashkenazi-Jewish and non-Jewish adult GM2 gangliosidosis patients share a common genetic defectR Navon, E H Kolodny, H Mitsumoto, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Is the WKL1 gene associated with schizophrenia?M Kaganovich, A Peretz, M Ritsner, et al.American Journal of Human Genetics|November 1, 1981
Hereditary heat-labile hexosaminidase B: its implication for recognizing Tay-Sachs genotypesR Navon, J Nutman, R Kopel, et al.Pageof 5