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The Journal of Clinical Investigation|September 1, 1975
Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiencyG C Tsay, G Dawson, R MatalonJournal of the American Dental Association (1939)|December 1, 1983
Delayed dental age in hepatorenal glycogen storage diseaseH T Loevy, R Matalon, I M RosenthalOphthalmology|February 1, 1986
Galactokinase activity in patients with idiopathic cataractsM J Elman, M T Miller, R MatalonBiomedical & Environmental Mass Spectrometry|October 1, 1988
Analysis of the pentafluorobenzoyl derivative of phenylethylamine utilizing negative ion chemical ionization and gas chromatography/mass spectrometryP Gashkoff, R Matalon, V Papa, et al.American Journal of Medical Genetics|August 1, 1990
Transmission of ring 14 chromosome from mother to two sonsR Matalon, P Supple, H Wyandt, et al.Nature Genetics|October 1, 1993
Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan diseaseR Kaul, G P Gao, K Balamurugan, et al.Journal of Craniofacial Genetics and Developmental Biology|January 1, 1985
Craniofacial and mucopolysaccharide abnormalities in Kniest dysplasiaH Friede, R Matalon, V Harris, et al.Gene Therapy|August 1, 1995
Overexpression of arylsulfatase A gene in fibroblasts from metachromatic leukodystrophy patients does not induce a new phenotypeT Ohashi, R Matalon, J A Barranger, et al.Genomics|May 15, 1994
Canavan disease: genomic organization and localization of human ASPA to 17p13-ter and conservation of the ASPA gene during evolutionR Kaul, K Balamurugan, G P Gao, et al.Annales De Genetique|September 22, 2000
Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndromeG V Velagaleti, A Kumar, L H Lockhart, et al.Pageof 13