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J T Hecht

Showing results (71-80 of 104) with videos related to

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Osteoarthritis and Cartilage|August 17, 2011
Comparative analysis with collagen type II distinguishes cartilage oligomeric matrix protein as a primary TGFβ-responsive geneH Li, D R Haudenschild, K L Posey, et al.
Genomics|June 14, 2000
Confirmation of the mapping of the Camurati-Englemann locus to 19q13. 2 and refinement to a 3.2-cM regionS P Vaughn, S Broussard, C R Hall, et al.
American Journal of Human Genetics|January 1, 1996
Exclusion of linkage between cleft lip with or without cleft palate and markers on chromosomes 4 and 6S H Blanton, E Crowder, S Malcolm, et al.
Genomics|November 26, 1998
Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palateK Yoshiura, J Machida, S Daack-Hirsch, et al.
American Journal of Medical Genetics|April 17, 1999
Neuroanatomic and neuropsychological outcome in school-age children with achondroplasiaN M Thompson, J T Hecht, T P Bohan, et al.
Nature Genetics|September 1, 1996
The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genesD Stickens, G Clines, D Burbee, 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.
American Journal of Medical Genetics|November 1, 1992
Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasiaJ T Hecht, S H Blanton, Y Wang, et al.
American Journal of Human Genetics|January 1, 1997
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignanciesJ T Hecht, D Hogue, Y Wang, et al.
Genomics|December 15, 1996
Characterization of human DSPG3, a small dermatan sulfate proteoglycanM Deere, J Johnson, S Garza, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Osteoarthritis and Cartilage|August 17, 2011
Comparative analysis with collagen type II distinguishes cartilage oligomeric matrix protein as a primary TGFβ-responsive geneH Li, D R Haudenschild, K L Posey, et al.
Genomics|June 14, 2000
Confirmation of the mapping of the Camurati-Englemann locus to 19q13. 2 and refinement to a 3.2-cM regionS P Vaughn, S Broussard, C R Hall, et al.
American Journal of Human Genetics|January 1, 1996
Exclusion of linkage between cleft lip with or without cleft palate and markers on chromosomes 4 and 6S H Blanton, E Crowder, S Malcolm, et al.
Genomics|November 26, 1998
Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palateK Yoshiura, J Machida, S Daack-Hirsch, et al.
American Journal of Medical Genetics|April 17, 1999
Neuroanatomic and neuropsychological outcome in school-age children with achondroplasiaN M Thompson, J T Hecht, T P Bohan, et al.
Nature Genetics|September 1, 1996
The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genesD Stickens, G Clines, D Burbee, 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.
American Journal of Medical Genetics|November 1, 1992
Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasiaJ T Hecht, S H Blanton, Y Wang, et al.
American Journal of Human Genetics|January 1, 1997
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignanciesJ T Hecht, D Hogue, Y Wang, et al.
Genomics|December 15, 1996
Characterization of human DSPG3, a small dermatan sulfate proteoglycanM Deere, J Johnson, S Garza, et al.
Pageof 11