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European Journal of Pediatrics|July 1, 1994
Phenotypic variability in the Baller-Gerold syndrome: report of a mildly affected patient and review of the literatureF J Ramos Fuentes, L Nicholson, C I ScottMatrix Biology : Journal of the International Society for Matrix Biology|January 29, 1999
Retention of cartilage oligomeric matrix protein (COMP) and cell death in redifferentiated pseudoachondroplasia chondrocytesJ T Hecht, D Montufar-Solis, G Decker, et al.American Journal of Medical Genetics|June 13, 1997
Mosaicism in pseudoachondroplasiaH L Ferguson, M Deere, R Evans, et al.Bone|July 12, 2002
Heparan sulfate abnormalities in exostosis growth platesJ T Hecht, C R Hall, M Snuggs, et al.American Journal of Human Genetics|September 1, 1991
Cleft lip and palate: no evidence of linkage to transforming growth factor alphaJ T Hecht, Y P Wang, S H Blanton, et al.American Journal of Medical Genetics|March 7, 1998
X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP)M E Hodes, A Hadjisavvas, I J Butler, et al.Annals of Neurology|April 18, 1998
Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonismA Brashear, I J Butler, K Hyland, et al.Biochemical Pharmacology|March 16, 2010
Biochemical alterations of dopamine receptor responses following chronic L-dopa therapyK D Wilner, I J Butler, W E Seifert, et al.Annals of Neurology|March 1, 1978
A disorder of biogenic amines in dihydropteridine reductase deficiencyI J Butler, S H Koslow, A Krumholz, et al.Pageof 21