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R Heilig

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Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
The New England Journal of Medicine|March 14, 1985
Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probeI Oberle, G Camerino, R Heilig, et al.
Human Genetics|January 1, 1985
First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probeJ Boué, I Oberle, R Heilig, et al.
Cytogenetic and Genome Research|November 20, 2002
Assignment of FUT8 to chicken chromosome band 5q1.4 and to human chromosome 14q23.2-->q24.1 by in situ hybridization. Conserved and compared synteny between human and chickenP Coullin, R P M A Crooijmans, M A M Groenen, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1984
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus)G Camerino, K H Grzeschik, M Jaye, et al.
Genomics|March 20, 1995
The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer diseaseD Campion, C Martin, R Heilig, et al.
Human Molecular Genetics|March 21, 1998
A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisisS Saunier, J Calado, R Heilig, et al.
Nucleic Acids Research|May 23, 2001
The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonisI Chambaud, R Heilig, S Ferris, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markersI Oberlé, R Heilig, J P Moisan, et al.
Mutation Research|November 3, 2001
Comprehensive analysis of a large genomic sequence at the putative B-cell chronic lymphocytic leukaemia (B-CLL) tumour suppresser gene locusG Rondeau, I Moreau, S Bézieau, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
The New England Journal of Medicine|March 14, 1985
Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probeI Oberle, G Camerino, R Heilig, et al.
Human Genetics|January 1, 1985
First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probeJ Boué, I Oberle, R Heilig, et al.
Cytogenetic and Genome Research|November 20, 2002
Assignment of FUT8 to chicken chromosome band 5q1.4 and to human chromosome 14q23.2-->q24.1 by in situ hybridization. Conserved and compared synteny between human and chickenP Coullin, R P M A Crooijmans, M A M Groenen, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1984
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus)G Camerino, K H Grzeschik, M Jaye, et al.
Genomics|March 20, 1995
The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer diseaseD Campion, C Martin, R Heilig, et al.
Human Molecular Genetics|March 21, 1998
A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisisS Saunier, J Calado, R Heilig, et al.
Nucleic Acids Research|May 23, 2001
The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonisI Chambaud, R Heilig, S Ferris, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markersI Oberlé, R Heilig, J P Moisan, et al.
Mutation Research|November 3, 2001
Comprehensive analysis of a large genomic sequence at the putative B-cell chronic lymphocytic leukaemia (B-CLL) tumour suppresser gene locusG Rondeau, I Moreau, S Bézieau, et al.
Pageof 5