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J T Hecht

Showing results (11-20 of 104) with videos related to

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Clinical Genetics|January 1, 1984
The Schinzel syndrome in a mother and daughterJ T Hecht, C I Scott
American Journal of Human Genetics|September 1, 1996
Nonsyndromic cleft lip with or without cleft palate: new BCL3 informationC Amos, D Gasser, J T Hecht
Human Molecular Genetics|December 1, 1992
Polymorphic dinucleotide repeat in a cartilage matrix protein (CRTM) geneY Wang, L Sadler, J T Hecht
American Journal of Medical Genetics|May 17, 1996
Natural history study of pseudoachondroplasiaJ McKeand, J Rotta, J T Hecht
Cell 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 Hecht
European Journal of Pediatrics|November 1, 1984
Long-term neurological sequelae in achondroplasiaJ T Hecht, I J Butler, C I Scott
The 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.
Human Molecular Genetics|August 1, 1993
Repeat polymorphisms in human fibrillin genes on chromosome 15 (FBN1) and chromosome 5 (FBN2)A L Biddinger, J T Hecht, D M Milewicz
American Journal of Medical Genetics|March 29, 1996
Standard weight for height curves in achondroplasiaA G Hunter, J T Hecht, C I Scott
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 Kurland
Pageof 11

Showing results (11-20 of 104) with videos related to

Sort By:
Pageof 11
Clinical Genetics|January 1, 1984
The Schinzel syndrome in a mother and daughterJ T Hecht, C I Scott
American Journal of Human Genetics|September 1, 1996
Nonsyndromic cleft lip with or without cleft palate: new BCL3 informationC Amos, D Gasser, J T Hecht
Human Molecular Genetics|December 1, 1992
Polymorphic dinucleotide repeat in a cartilage matrix protein (CRTM) geneY Wang, L Sadler, J T Hecht
American Journal of Medical Genetics|May 17, 1996
Natural history study of pseudoachondroplasiaJ McKeand, J Rotta, J T Hecht
Cell 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 Hecht
European Journal of Pediatrics|November 1, 1984
Long-term neurological sequelae in achondroplasiaJ T Hecht, I J Butler, C I Scott
The 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.
Human Molecular Genetics|August 1, 1993
Repeat polymorphisms in human fibrillin genes on chromosome 15 (FBN1) and chromosome 5 (FBN2)A L Biddinger, J T Hecht, D M Milewicz
American Journal of Medical Genetics|March 29, 1996
Standard weight for height curves in achondroplasiaA G Hunter, J T Hecht, C I Scott
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 Kurland
Pageof 11