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Epilepsia|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 HechtAmerican Journal of Medical Genetics|February 1, 1985
Computerized tomography of the foramen magnum: achondroplastic values compared to normal standardsJ T Hecht, F W Nelson, I J Butler, et al.American Journal of Medical Genetics|May 17, 1996
Natural history study of pseudoachondroplasiaJ McKeand, J Rotta, J T HechtClinical Orthopaedics and Related Research|January 11, 1976
Achondroplastic and hypochondroplastic dwarfismC I ScottBirth Defects Original Article Series|May 1, 1971
Unusual facies, joint hypermobility, genital anomaly and short stature: a new dysmorphic syndromeC I ScottCell Calcium|October 3, 2000
Delta 469 mutation in the type 3 repeat calcium binding domain of cartilage oligomeric matrix protein (COMP) disrupts calcium bindingJ Hou, J A Putkey, J T HechtThe Journal of Biological Chemistry|June 15, 2000
Cartilage oligomeric matrix protein is a calcium-binding protein, and a mutation in its type 3 repeats causes conformational changesH Chen, M Deere, J T Hecht, et al.American Journal of Medical Genetics|June 1, 1989
Epilepsy and clefting disorders: lack of evidence of a familial associationJ T Hecht, J F Annegers, L T KurlandPrenatal Diagnosis|March 1, 1994
Tibial hemimelia syndrome: prenatal diagnosis by real-time ultrasoundM Ramirez, J T Hecht, S Taylor, et al.Pageof 14