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Acta Neuropathologica|January 1, 1989
Striatal degeneration in glutaric acidaemia type IIC W Chow, F E Frerman, S I Goodman, et al.Biomedical Mass Spectrometry|October 1, 1979
Abnormal deoxyribose metabolites in the urine of a child with a possible new inborn error of metabolismR J Truscott, B Halpern, J Hammond, et al.American Journal of Medical Genetics|July 15, 1994
Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22A J Donnelly, K H Choo, H M Kozman, et al.Journal of Medical Genetics|January 1, 1993
The clinical features of spondyloepiphyseal dysplasia congenita resulting from the substitution of glycine 997 by serine in the alpha 1(II) chain of type II collagenW G Cole, R K Hall, J G RogersEuropean Journal of Pediatrics|September 4, 1998
Cerebrospinal fluid shunts in the management of behavioural problems in Sanfilippo syndrome (MPS III)S P Robertson, G L Klug, J G RogersThe Journal of Pediatrics|December 1, 1977
Use and complications of high-dose disodium etidronate therapy in fibrodysplasia ossificans progressivaJ G Rogers, J P Dorst, W B GehoAmerican Journal of Medical Genetics|August 1, 1988
Duplication of a small segment of 5p due to maternal recombination within a paracentric shiftG C Webb, L E Voullaire, J G RogersJournal of Medical Genetics|February 1, 1988
Absence of a lateral rectus muscle associated with duplication of the chromosome segment 7q32----q34C G Keith, G C Webb, J G RogersThe Journal of Pediatrics|January 1, 1979
Familial syndrome of mental retardation, short stature, contractures of the hands, and genital anomaliesM D Urban, J G Rogers, W J MeyerAmerican Journal of Obstetrics and Gynecology|April 15, 1985
Treatment of placental vasculature with a neodymium-yttrium-aluminum-garnet laser via fetoscopyJ E DeLia, J G Rogers, J A DixonPageof 19