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C A Francomano

Showing results (1-10 of 101) with videos related to

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Nature Genetics|January 1, 1995
Key role for a minor collagenC A Francomano
Pediatric Nephrology (Berlin, Germany)|January 1, 1992
Diagnostic approaches to renal genetic disorders using DNA analysisC A Francomano
The New England Journal of Medicine|January 5, 1995
The genetic basis of dwarfismC A Francomano
Annual Review of Medicine|January 1, 1986
DNA analysis in genetic disordersC A Francomano, H H Kazazian
Genomics|December 28, 1999
Characterization of the human talin (TLN) gene: genomic structure, chromosomal localization, and expression patternT Ben-Yosef, C A Francomano
Genomics|February 13, 2001
Characterization of a human gene encoding nucleosomal binding protein NSBP1L M King, C A Francomano
American Journal of Medical Genetics|April 1, 1988
Achondroplasia is not caused by mutation in the gene for type II collagenC A Francomano, R E Pyeritz
Nucleic Acids Research|March 11, 1991
PCR-based detection of polymorphic DdeI and KpnI sites in intron 5 of the adenylate kinase (AK1) geneE G Puffenberger, C A Francomano
Human Mutation|January 1, 1995
Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagenI McIntosh, M H Abbott, C A Francomano
Endocrine Reviews|March 4, 2000
The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricansZ Vajo, C A Francomano, D J Wilkin
Pageof 11

Showing results (1-10 of 101) with videos related to

Sort By:
Pageof 11
Nature Genetics|January 1, 1995
Key role for a minor collagenC A Francomano
Pediatric Nephrology (Berlin, Germany)|January 1, 1992
Diagnostic approaches to renal genetic disorders using DNA analysisC A Francomano
The New England Journal of Medicine|January 5, 1995
The genetic basis of dwarfismC A Francomano
Annual Review of Medicine|January 1, 1986
DNA analysis in genetic disordersC A Francomano, H H Kazazian
Genomics|December 28, 1999
Characterization of the human talin (TLN) gene: genomic structure, chromosomal localization, and expression patternT Ben-Yosef, C A Francomano
Genomics|February 13, 2001
Characterization of a human gene encoding nucleosomal binding protein NSBP1L M King, C A Francomano
American Journal of Medical Genetics|April 1, 1988
Achondroplasia is not caused by mutation in the gene for type II collagenC A Francomano, R E Pyeritz
Nucleic Acids Research|March 11, 1991
PCR-based detection of polymorphic DdeI and KpnI sites in intron 5 of the adenylate kinase (AK1) geneE G Puffenberger, C A Francomano
Human Mutation|January 1, 1995
Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagenI McIntosh, M H Abbott, C A Francomano
Endocrine Reviews|March 4, 2000
The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricansZ Vajo, C A Francomano, D J Wilkin
Pageof 11