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C A Francomano

Showing results (21-30 of 101) with videos related to

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Genomics|May 20, 1995
Localization of the gene (SYM1) for proximal symphalangism to human chromosome 17q21-q22M H Polymeropoulos, J Poush, J R Rubenstein, et al.
American Journal of Medical Genetics|February 1, 1988
Marfan syndrome: exclusion of genetic linkage to three major collagen genesC A Francomano, E A Streeten, D A Meyers, et al.
American Journal of Human Genetics|September 1, 1987
Mortality in achondroplasiaJ T Hecht, C A Francomano, W A Horton, et al.
Genomics|June 1, 1990
Use of denaturing gradient gel electrophoresis for detection of mutation and prospective diagnosis in late onset ornithine transcarbamylase deficiencyJ E Finkelstein, C A Francomano, S W Brusilow, 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.
Lancet (London, England)|December 7, 1991
DNA light on the Tegernsee giantW F Schwindinger, C A Francomano, M A Levine, et al.
Clinical Genetics|October 31, 2001
Living with Marfan syndrome II. Medication adherence and physical activity modificationK F Peters, R Horne, F Kong, et al.
Human Molecular Genetics|May 23, 1998
Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VIS Chang, M J Rosenberg, H Morton, et al.
Clinical Genetics|October 31, 2001
Living with Marfan syndrome I. Perceptions of the conditionK F Peters, F Kong, R Horne, et al.
American Journal of Medical Genetics|March 14, 2002
Comprehensive resource: Skeletal gene databaseL Jia, N C Ho, S S Park, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
Genomics|May 20, 1995
Localization of the gene (SYM1) for proximal symphalangism to human chromosome 17q21-q22M H Polymeropoulos, J Poush, J R Rubenstein, et al.
American Journal of Medical Genetics|February 1, 1988
Marfan syndrome: exclusion of genetic linkage to three major collagen genesC A Francomano, E A Streeten, D A Meyers, et al.
American Journal of Human Genetics|September 1, 1987
Mortality in achondroplasiaJ T Hecht, C A Francomano, W A Horton, et al.
Genomics|June 1, 1990
Use of denaturing gradient gel electrophoresis for detection of mutation and prospective diagnosis in late onset ornithine transcarbamylase deficiencyJ E Finkelstein, C A Francomano, S W Brusilow, 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.
Lancet (London, England)|December 7, 1991
DNA light on the Tegernsee giantW F Schwindinger, C A Francomano, M A Levine, et al.
Clinical Genetics|October 31, 2001
Living with Marfan syndrome II. Medication adherence and physical activity modificationK F Peters, R Horne, F Kong, et al.
Human Molecular Genetics|May 23, 1998
Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VIS Chang, M J Rosenberg, H Morton, et al.
Clinical Genetics|October 31, 2001
Living with Marfan syndrome I. Perceptions of the conditionK F Peters, F Kong, R Horne, et al.
American Journal of Medical Genetics|March 14, 2002
Comprehensive resource: Skeletal gene databaseL Jia, N C Ho, S S Park, et al.
Pageof 11