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R Heilig

Showing results (41-50 of 50) with videos related to

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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.
Genomics|September 24, 1999
A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegiaJ Hazan, C S Davoine, D Mavel, et al.
Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.
Leukemia|October 6, 2001
A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemiaO A Bernard, M Busson-LeConiat, P Ballerini, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Nature|March 10, 2001
A physical map of human chromosome 14T Brüls, G Gyapay, J L Petit, et al.
Nature|March 10, 2001
A physical map of the human genomeJ D McPherson, M Marra, L Hillier, et al.
Nature|March 10, 2001
Initial sequencing and analysis of the human genomeE S Lander, L M Linton, B Birren, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
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.
Genomics|September 24, 1999
A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegiaJ Hazan, C S Davoine, D Mavel, et al.
Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.
Leukemia|October 6, 2001
A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemiaO A Bernard, M Busson-LeConiat, P Ballerini, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Nature|March 10, 2001
A physical map of human chromosome 14T Brüls, G Gyapay, J L Petit, et al.
Nature|March 10, 2001
A physical map of the human genomeJ D McPherson, M Marra, L Hillier, et al.
Nature|March 10, 2001
Initial sequencing and analysis of the human genomeE S Lander, L M Linton, B Birren, et al.
Pageof 5