Showing results (21-30 of 138) with videos related to
Sort By:
Pageof 14
American Journal of Medical Genetics|January 2, 1995
Natural history study of hereditary multiple exostosesC L Wicklund, R M Pauli, D Johnston, et al.The Journal of Bone and Joint Surgery. American Volume|March 1, 1982
Dyggve-Melchior-Clausen syndrome. A histochemical study of the growth plateW A Horton, C I ScottClinical Genetics|March 21, 2002
Familial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4C R Hall, Y Wu, L G Shaffer, et al.American Journal of Medical Genetics|March 1, 1993
Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardationL G Shaffer, J T Hecht, D H Ledbetter, et al.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.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.Pageof 14