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Annals of Neurology|January 1, 1980
Central core disease and malignant hyperthermia syndromeJ P Frank, Y Harati, I J Butler, et al.American Journal of Human Genetics|March 1, 1995
Genetic heterogeneity in multiple epiphyseal dysplasiaM Deere, S H Blanton, C I Scott, et al.European Journal of Pediatrics|December 1, 1986
Foramen magnum stenosis in homozygous achondroplasiaJ T Hecht, W A Horton, I J Butler, et al.The New England Journal of Medicine|July 19, 1984
Progressive neurologic deterioration and renal failure due to storage of glutamyl ribose-5-phosphateJ C Williams, I J Butler, H S Rosenberg, et al.American Journal of Human Genetics|April 1, 1992
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypesG A Greenhaw, A Hebert, M E Duke-Woodside, et al.American Journal of Medical Genetics|March 14, 2002
Pseudoachondroplasia and multiple epiphyseal dysplasia: New etiologic developmentsS Unger, J T HechtEpilepsia|September 1, 1990
Familial aggregation of epilepsy and clefting disorders: a review of the literatureJ T Hecht, J F AnnegersCurrent Drug Targets|October 16, 2008
The role of cartilage oligomeric matrix protein (COMP) in skeletal diseaseK L Posey, J T HechtPageof 21