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B Weiffenbach

Showing results (31-40 of 42) with videos related to

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Gastroenterology|July 1, 1991
Genetic characterization of the APC locus involved in familial adenomatous polyposisS Olschwang, B Weiffenbach, P Laurent-Puig, et al.
Molecular Endocrinology (Baltimore, Md.)|June 1, 1990
Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20M L Summar, J A Phillips, J Battey, et al.
Nature Genetics|June 1, 1993
Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination eventsB Weiffenbach, J Dubois, D Storvick, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHDB Weiffenbach, R G Bagley, K Falls, et al.
American Journal of Human Genetics|August 1, 1992
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35B Weiffenbach, R Bagley, K Falls, et al.
Cell|October 23, 1987
A genetic linkage map of the human genomeH Donis-Keller, P Green, C Helms, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 1998
Genetic polymorphism of CYP2D6 and lung cancer riskG L Shaw, R T Falk, J N Frame, et al.
The American Journal of Psychiatry|May 18, 1999
Dopamine D4 gene 7-repeat allele and attention deficit hyperactivity disorderS V Faraone, J Biederman, B Weiffenbach, et al.
Genomics|February 1, 1994
YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) geneB Weiffenbach, J Dubois, S Manning, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Gastroenterology|July 1, 1991
Genetic characterization of the APC locus involved in familial adenomatous polyposisS Olschwang, B Weiffenbach, P Laurent-Puig, et al.
Molecular Endocrinology (Baltimore, Md.)|June 1, 1990
Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20M L Summar, J A Phillips, J Battey, et al.
Nature Genetics|June 1, 1993
Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination eventsB Weiffenbach, J Dubois, D Storvick, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHDB Weiffenbach, R G Bagley, K Falls, et al.
American Journal of Human Genetics|August 1, 1992
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35B Weiffenbach, R Bagley, K Falls, et al.
Cell|October 23, 1987
A genetic linkage map of the human genomeH Donis-Keller, P Green, C Helms, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 1998
Genetic polymorphism of CYP2D6 and lung cancer riskG L Shaw, R T Falk, J N Frame, et al.
The American Journal of Psychiatry|May 18, 1999
Dopamine D4 gene 7-repeat allele and attention deficit hyperactivity disorderS V Faraone, J Biederman, B Weiffenbach, et al.
Genomics|February 1, 1994
YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) geneB Weiffenbach, J Dubois, S Manning, et al.
Pageof 5