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Journal of Medical Genetics|October 11, 1976
Discordance for Cornelia de Lange syndrome in twinsR E Stevenson, C I ScottAmerican Journal of Human Genetics|September 1, 1991
Complex segregation analysis of nonsyndromic cleft lip and palateJ T Hecht, P Yang, V V Michels, et al.American Journal of Medical Genetics|September 19, 1998
Genetic epidemiology study of idiopathic talipes equinovarusC Lochmiller, D Johnston, A Scott, et al.Annals of Neurology|March 1, 1983
A dominantly inherited syndrome with continuous motor neuron dischargesT Ashizawa, I J Butler, Y Harati, et al.Apoptosis : an International Journal on Programmed Cell Death|May 27, 2003
Apoptosis staining in cultured pseudoachondroplasia chondrocytesJ Duke, D Montufar-Solis, S Underwood, et al.American Journal of Human Genetics|September 1, 1987
Mortality in achondroplasiaJ T Hecht, C A Francomano, W A Horton, et al.American Journal of Medical Genetics|January 8, 1999
Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasiaM Deere, T Sanford, H L Ferguson, et al.Journal of Child Neurology|April 9, 2001
Encephalopathy associated with respiratory syncytial virus bronchiolitisY T Ng, C Cox, J Atkins, et al.American Journal of Medical Genetics|July 16, 1999
Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasiaM Deere, T Sanford, C A Francomano, et al.American Journal of Medical Genetics|June 13, 1997
Extended survival in a new case of ter Haar syndrome: further delineation of the syndromeR Wallerstein, C I Scott, L NicholsonPageof 21