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Altherr

Showing results (101-110 of 127) with videos related to

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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.
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.
Human Genetics|September 1, 1993
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locusC Wijmenga, S T Winokur, G W Padberg, et al.
Human Molecular Genetics|June 9, 1998
WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myelomaI Stec, T J Wright, G J van Ommen, et al.
American Journal of Medical Genetics|September 5, 1997
High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndromeY Y Fang, S Bain, E A Haan, et al.
Conservation Biology : the Journal of the Society for Conservation Biology|September 3, 2021
The dangers of misrepresenting wildlife trade: response to Natusch et al. 2021David P Edwards, Neil D'Cruze, Sandra Altherr, et al.
Genomics|May 1, 1992
Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate regionJ F Gusella, M R Altherr, A I McClatchey, et al.
Somatic Cell and Molecular Genetics|September 1, 1991
New DNA markers in the Huntington's disease gene candidate regionC S Lin, M Altherr, G Bates, et al.
Health Security|August 22, 2019
Development of a Supervised Learning Algorithm for Detection of Potential Disease Reemergence: A Proof of ConceptManeesha Chitanvis, Ashlynn R Daughton, Forest Altherr, et al.
Human Molecular Genetics|May 1, 1997
Reduced penetrance of the Huntington's disease mutationS M McNeil, A Novelletto, J Srinidhi, et al.
Pageof 13

Showing results (101-110 of 127) with videos related to

Sort By:
Pageof 13
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.
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.
Human Genetics|September 1, 1993
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locusC Wijmenga, S T Winokur, G W Padberg, et al.
Human Molecular Genetics|June 9, 1998
WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myelomaI Stec, T J Wright, G J van Ommen, et al.
American Journal of Medical Genetics|September 5, 1997
High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndromeY Y Fang, S Bain, E A Haan, et al.
Conservation Biology : the Journal of the Society for Conservation Biology|September 3, 2021
The dangers of misrepresenting wildlife trade: response to Natusch et al. 2021David P Edwards, Neil D'Cruze, Sandra Altherr, et al.
Genomics|May 1, 1992
Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate regionJ F Gusella, M R Altherr, A I McClatchey, et al.
Somatic Cell and Molecular Genetics|September 1, 1991
New DNA markers in the Huntington's disease gene candidate regionC S Lin, M Altherr, G Bates, et al.
Health Security|August 22, 2019
Development of a Supervised Learning Algorithm for Detection of Potential Disease Reemergence: A Proof of ConceptManeesha Chitanvis, Ashlynn R Daughton, Forest Altherr, et al.
Human Molecular Genetics|May 1, 1997
Reduced penetrance of the Huntington's disease mutationS M McNeil, A Novelletto, J Srinidhi, et al.
Pageof 13