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C A Francomano

Showing results (71-80 of 101) with videos related to

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Genomics|February 10, 1995
COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type IID S Greenspan, H Northrup, K S Au, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|December 1, 1992
Atopy and bronchial hyperresponsiveness: exclusion of linkage to markers on chromosomes 11q and 6pP J Amelung, C I Panhuysen, D S Postma, et al.
Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.
Nature Genetics|September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaM L Warman, M Abbott, S S Apte, et al.
American Journal of Medical Genetics|December 15, 1994
Report from the Maryland Epidemiology Schizophrenia Linkage Study: no evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant modelM Karayiorgou, L Kasch, V K Lasseter, et al.
Human Molecular Genetics|April 18, 1998
Genetic and physical mapping of the McKusick-Kaufman syndromeD L Stone, R Agarwala, A A Schäffer, et al.
American Journal of Human Genetics|September 1, 1991
Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the geneK Kainulainen, B Steinmann, F Collins, et al.
American Journal of Human Genetics|August 23, 2000
A novel nemaline myopathy in the Amish caused by a mutation in troponin T1J J Johnston, R I Kelley, T O Crawford, et al.
Spine|February 27, 2001
Thoracolumbar spinal abnormalities in Stickler syndromeP S Rose, N U Ahn, H P Levy, et al.
Nature Genetics|July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaG A Bellus, I McIntosh, E A Smith, et al.
Pageof 11

Showing results (71-80 of 101) with videos related to

Sort By:
Pageof 11
Genomics|February 10, 1995
COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type IID S Greenspan, H Northrup, K S Au, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|December 1, 1992
Atopy and bronchial hyperresponsiveness: exclusion of linkage to markers on chromosomes 11q and 6pP J Amelung, C I Panhuysen, D S Postma, et al.
Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.
Nature Genetics|September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaM L Warman, M Abbott, S S Apte, et al.
American Journal of Medical Genetics|December 15, 1994
Report from the Maryland Epidemiology Schizophrenia Linkage Study: no evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant modelM Karayiorgou, L Kasch, V K Lasseter, et al.
Human Molecular Genetics|April 18, 1998
Genetic and physical mapping of the McKusick-Kaufman syndromeD L Stone, R Agarwala, A A Schäffer, et al.
American Journal of Human Genetics|September 1, 1991
Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the geneK Kainulainen, B Steinmann, F Collins, et al.
American Journal of Human Genetics|August 23, 2000
A novel nemaline myopathy in the Amish caused by a mutation in troponin T1J J Johnston, R I Kelley, T O Crawford, et al.
Spine|February 27, 2001
Thoracolumbar spinal abnormalities in Stickler syndromeP S Rose, N U Ahn, H P Levy, et al.
Nature Genetics|July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaG A Bellus, I McIntosh, E A Smith, et al.
Pageof 11