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J T Hecht

Showing results (61-70 of 104) with videos related to

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American Journal of Human Genetics|May 1, 1995
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, 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.
Annals of Neurology|July 1, 1988
Neurological basis of respiratory complications in achondroplasiaF W Nelson, J T Hecht, W A Horton, et al.
Neurology|November 18, 1998
Expanding the phenotype of the 8344 transfer RNAlysine mitochondrial DNA mutationS A Austin, F J Vriesendorp, F T Thandroyen, et al.
American Journal of Medical Genetics|November 1, 1988
Obesity in achondroplasiaJ T Hecht, O J Hood, R J Schwartz, et al.
American Journal of Medical Genetics|September 19, 1998
Segregation analysis of idiopathic talipes equinovarus in a Texan populationM de Andrade, J S Barnholtz, C I Amos, et al.
Genome Research|May 18, 1999
Genomic characterization of human DSPG3M Deere, J L Dieguez, S J Yoon, et al.
American Journal of Medical Genetics|July 3, 1995
Confirmatory linkage of hypochondroplasia to chromosome arm 4pJ T Hecht, C A Herrera, G A Greenhaw, et al.
Journal of Medical Genetics|April 16, 2002
DTDST mutations are not a frequent cause of idiopathic talipes equinovarus (club foot)L Bonafé, S H Blanton, A Scott, et al.
American Journal of Medical Genetics|March 1, 1992
Growth hormone therapy in achondroplasiaW A Horton, J T Hecht, O J Hood, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|May 1, 1995
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, 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.
Annals of Neurology|July 1, 1988
Neurological basis of respiratory complications in achondroplasiaF W Nelson, J T Hecht, W A Horton, et al.
Neurology|November 18, 1998
Expanding the phenotype of the 8344 transfer RNAlysine mitochondrial DNA mutationS A Austin, F J Vriesendorp, F T Thandroyen, et al.
American Journal of Medical Genetics|November 1, 1988
Obesity in achondroplasiaJ T Hecht, O J Hood, R J Schwartz, et al.
American Journal of Medical Genetics|September 19, 1998
Segregation analysis of idiopathic talipes equinovarus in a Texan populationM de Andrade, J S Barnholtz, C I Amos, et al.
Genome Research|May 18, 1999
Genomic characterization of human DSPG3M Deere, J L Dieguez, S J Yoon, et al.
American Journal of Medical Genetics|July 3, 1995
Confirmatory linkage of hypochondroplasia to chromosome arm 4pJ T Hecht, C A Herrera, G A Greenhaw, et al.
Journal of Medical Genetics|April 16, 2002
DTDST mutations are not a frequent cause of idiopathic talipes equinovarus (club foot)L Bonafé, S H Blanton, A Scott, et al.
American Journal of Medical Genetics|March 1, 1992
Growth hormone therapy in achondroplasiaW A Horton, J T Hecht, O J Hood, et al.
Pageof 11