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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.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.Pageof 12