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Brain & Development|September 1, 1996
Two novel mutations in a Japanese patient with the late-infantile form of metachromatic leukodystrophyT Tsuda, Y Hasegawa, Y EtoPediatric Neurology|November 13, 2001
Magnetic resonance imaging in three children with kernicterusS Sugama, A Soeda, Y EtoEuropean Journal of Pediatrics|November 1, 1979
Urinary acid mucopolysaccharides in multiple sulfatase deficiency (mucosulfatidosis)Y Eto, S Numaguchi, T HandaJournal of Craniofacial Genetics and Developmental Biology|March 24, 2000
Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2M Tsukuno, H Suzuki, Y EtoBone|August 24, 1999
Local administration of activin promotes fracture healing in the rat fibula fracture modelR Sakai, K Miwa, Y EtoEndocrine Journal|February 1, 1995
Expression of immunoreactive activin A in fetal rat pancreasM Furukawa, Y Eto, I KojimaClinica Chimica Acta; International Journal of Clinical Chemistry|April 17, 1978
Effects of macromolecular compounds on human leukocyte beta-galactosidase activityK Kiguchi, Y Eto, K AokiHuman Mutation|January 1, 1993
Molecular screening of Japanese patients with Gaucher disease: phenotypic variability in the same genotypesH Kawame, K Maekawa, Y EtoDNA and Cell Biology|July 1, 1993
Mutations in the arylsulfatase A gene of Japanese patients with metachromatic leukodystrophyY Hasegawa, H Kawame, Y EtoNihon Rinsho. Japanese Journal of Clinical Medicine|September 1, 1993
[Molecular analysis of Japanese patients with metachromatic leukodystrophy]Y Hasegawa, H Kawame, Y EtoPageof 55