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American Journal of Medical Genetics|May 1, 1988
Simpson-Golabi-Behmel syndrome: follow-up of the Michigan familyJ M Opitz, J Herrmann, E F Gilbert, et al.Clinical Genetics|February 1, 1986
Sanfilippo disease in GreeceN G Beratis, S L Sklower, L Wilbur, et al.Prenatal Diagnosis|January 1, 2024
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20CCourtney P Verscaj, Carly Smith, Margaret Homeyer, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1994
Lipoprotein glomerulopathy: first report in a Chinese maleP Zhang, R Matalon, L Kaplan, et al.Science (New York, N.Y.)|August 31, 1973
N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycansJ N Thompson, A C Stoolmiller, R Matalon, et al.European Journal of Pediatrics|July 1, 1996
Nutrition and reproductive outcome in maternal phenylketonuriaK Michals, P B Acosta, V Austin, et al.American Journal of Diseases of Children (1960)|July 1, 1987
Phenotypic features of patients with congenital adrenal hypoplasia and glycerol kinase deficiencyJ E Wise, R Matalon, A M Morgan, et al.Journal of Neurochemistry|January 1, 1991
Purification, characterization, and localization of aspartoacylase from bovine brainR Kaul, J Casanova, A B Johnson, et al.Genomics|August 22, 2000
Canine heparan sulfate sulfamidase and the molecular pathology underlying Sanfilippo syndrome type A in DachshundsE L Aronovich, K P Carmichael, H Morizono, et al.Indian Journal of Pediatrics|January 1, 1990
Plasma amino acid patterns in very low birth weight infants during parenteral nutritionG Srinivasan, A Amin, R S Pildes, et al.Pageof 13