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A D Børglum

Showing results (1-10 of 44) with videos related to

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Allergy|December 17, 2003
Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and XpA Haagerup, A D Børglum, H G Binderup, et al.
Human Genetics|January 1, 1997
Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysisA D Børglum, T Flint, L L Hansen, et al.
Human Genetics|July 1, 1992
Two PstI polymorphisms for the urokinase-type plasminogen activator receptor gene (PLAUR)A D Børglum, A Byskov, A L Roldan, et al.
Journal of Medical Genetics|March 10, 2006
Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseasesC Brasch-Andersen, A Haagerup, A D Børglum, et al.
Human Genetics|November 1, 1995
Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21A D Børglum, T Flint, P Madsen, et al.
Clinical Genetics|October 1, 1994
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplicationJ M Hertz, A D Børglum, C A Brandt, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32A D Børglum, T Flint, N Tommerup, et al.
Thorax|August 7, 2008
Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disordersS Møller-Larsen, M Nyegaard, A Haagerup, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Two-dimensional DNA typing as a genetic marker system in humansA D Børglum, E Mullaart, A B Kvistgaard, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
A new locus for Seckel syndrome on chromosome 18p11.31-q11.2A D Børglum, T Balslev, A Haagerup, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Allergy|December 17, 2003
Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and XpA Haagerup, A D Børglum, H G Binderup, et al.
Human Genetics|January 1, 1997
Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysisA D Børglum, T Flint, L L Hansen, et al.
Human Genetics|July 1, 1992
Two PstI polymorphisms for the urokinase-type plasminogen activator receptor gene (PLAUR)A D Børglum, A Byskov, A L Roldan, et al.
Journal of Medical Genetics|March 10, 2006
Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseasesC Brasch-Andersen, A Haagerup, A D Børglum, et al.
Human Genetics|November 1, 1995
Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21A D Børglum, T Flint, P Madsen, et al.
Clinical Genetics|October 1, 1994
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplicationJ M Hertz, A D Børglum, C A Brandt, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32A D Børglum, T Flint, N Tommerup, et al.
Thorax|August 7, 2008
Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disordersS Møller-Larsen, M Nyegaard, A Haagerup, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Two-dimensional DNA typing as a genetic marker system in humansA D Børglum, E Mullaart, A B Kvistgaard, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
A new locus for Seckel syndrome on chromosome 18p11.31-q11.2A D Børglum, T Balslev, A Haagerup, et al.
Pageof 5