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C A Francomano

Showing results (81-90 of 101) with videos related to

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American Journal of Human Genetics|July 1, 1993
Genetic heterogeneity in families with hereditary multiple exostosesA Cook, W Raskind, S H Blanton, et al.
American Journal of Human Genetics|January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasiaJ E Finkelstein, K Doege, Y Yamada, et al.
American Journal of Human Genetics|February 1, 1995
Achondroplasia is defined by recurrent G380R mutations of FGFR3G A Bellus, T W Hefferon, R I Ortiz de Luna, et al.
Genomics|July 1, 1996
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16M H Polymeropoulos, S E Ide, M Wright, et al.
Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.
JAMA|September 18, 1996
Career development for women in academic medicine: Multiple interventions in a department of medicineL P Fried, C A Francomano, S M MacDonald, et al.
Journal of Medical Genetics|February 1, 1990
An exclusion map of Marfan syndromeS H Blanton, M Sarfarazi, H Eiberg, et al.
The Journal of Clinical Investigation|May 11, 1992
Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin geneH C Dietz, R E Pyeritz, E G Puffenberger, et al.
American Journal of Medical Genetics|July 16, 1999
Small deletions in the type II collagen triple helix produce kniest dysplasiaD J Wilkin, A S Artz, S South, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosomeD J Wilkin, J K Szabo, R Cameron, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|July 1, 1993
Genetic heterogeneity in families with hereditary multiple exostosesA Cook, W Raskind, S H Blanton, et al.
American Journal of Human Genetics|January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasiaJ E Finkelstein, K Doege, Y Yamada, et al.
American Journal of Human Genetics|February 1, 1995
Achondroplasia is defined by recurrent G380R mutations of FGFR3G A Bellus, T W Hefferon, R I Ortiz de Luna, et al.
Genomics|July 1, 1996
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16M H Polymeropoulos, S E Ide, M Wright, et al.
Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.
JAMA|September 18, 1996
Career development for women in academic medicine: Multiple interventions in a department of medicineL P Fried, C A Francomano, S M MacDonald, et al.
Journal of Medical Genetics|February 1, 1990
An exclusion map of Marfan syndromeS H Blanton, M Sarfarazi, H Eiberg, et al.
The Journal of Clinical Investigation|May 11, 1992
Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin geneH C Dietz, R E Pyeritz, E G Puffenberger, et al.
American Journal of Medical Genetics|July 16, 1999
Small deletions in the type II collagen triple helix produce kniest dysplasiaD J Wilkin, A S Artz, S South, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosomeD J Wilkin, J K Szabo, R Cameron, et al.
Pageof 11