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R HEILIG

Showing results (51-60 of 67) with videos related to

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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.
American Journal of Medical Genetics|July 9, 1999
Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1A Carrié, V Nepotes, P Billuart, 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.
Human Molecular Genetics|April 4, 2001
Mutations in the gene encoding SLURP-1 in Mal de MeledaJ Fischer, B Bouadjar, R Heilig, et al.
American Journal of Human Genetics|October 9, 2001
Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndromeC Lefèvre, F Jobard, F Caux, et al.
Genomics|July 8, 1998
A transcriptional Map of the FMF regionA Bernot, R Heilig, C Clepet, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
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.
American Journal of Medical Genetics|July 9, 1999
Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1A Carrié, V Nepotes, P Billuart, 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.
Human Molecular Genetics|April 4, 2001
Mutations in the gene encoding SLURP-1 in Mal de MeledaJ Fischer, B Bouadjar, R Heilig, et al.
American Journal of Human Genetics|October 9, 2001
Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndromeC Lefèvre, F Jobard, F Caux, et al.
Genomics|July 8, 1998
A transcriptional Map of the FMF regionA Bernot, R Heilig, C Clepet, et al.
Pageof 7