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G Brunner

Showing results (381-390 of 727) with videos related to

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American Journal of Medical Genetics|July 13, 2002
Expanding phenotype of XNP mutations: mild to moderate mental retardationHelger G Yntema, Francis A Poppelaars, Esther Derksen, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
American Journal of Human Genetics|March 19, 2021
The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effectsHila Fridman, Helger G Yntema, Reedik Mägi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 31, 2002
High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancerN Hoogerbrugge, P Bult, L M de Widt-Levert, et al.
Genomics|June 22, 1999
Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.
American Journal of Medical Genetics|March 13, 1995
Further delineation of the branchio-oculo-facial syndromeA E Lin, R J Gorlin, I W Lurie, et al.
Investigative Ophthalmology & Visual Science|October 18, 2014
Identification of adult stem cells in Schwalbe's line region of the primate eyeBarbara M Braunger, Bahar Ademoglu, Sebastian E Koschade, et al.
Genomics|August 1, 1993
Identification of four novel mutations in the COL4A5 gene of patients with Alport syndromeH H Lemmink, C H Schröder, H G Brunner, et al.
International Journal of Obesity (2005)|June 5, 2015
Intermuscular and perimuscular fat expansion in obesity correlates with skeletal muscle T cell and macrophage infiltration and insulin resistanceI M Khan, X Yd Perrard, G Brunner, et al.
Genomics|October 8, 1999
Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomaliesM E Gallardo, J Lopez-Rios, I Fernaud-Espinosa, et al.
Pageof 73

Showing results (381-390 of 727) with videos related to

Sort By:
Pageof 73
American Journal of Medical Genetics|July 13, 2002
Expanding phenotype of XNP mutations: mild to moderate mental retardationHelger G Yntema, Francis A Poppelaars, Esther Derksen, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
American Journal of Human Genetics|March 19, 2021
The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effectsHila Fridman, Helger G Yntema, Reedik Mägi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 31, 2002
High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancerN Hoogerbrugge, P Bult, L M de Widt-Levert, et al.
Genomics|June 22, 1999
Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.
American Journal of Medical Genetics|March 13, 1995
Further delineation of the branchio-oculo-facial syndromeA E Lin, R J Gorlin, I W Lurie, et al.
Investigative Ophthalmology & Visual Science|October 18, 2014
Identification of adult stem cells in Schwalbe's line region of the primate eyeBarbara M Braunger, Bahar Ademoglu, Sebastian E Koschade, et al.
Genomics|August 1, 1993
Identification of four novel mutations in the COL4A5 gene of patients with Alport syndromeH H Lemmink, C H Schröder, H G Brunner, et al.
International Journal of Obesity (2005)|June 5, 2015
Intermuscular and perimuscular fat expansion in obesity correlates with skeletal muscle T cell and macrophage infiltration and insulin resistanceI M Khan, X Yd Perrard, G Brunner, et al.
Genomics|October 8, 1999
Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomaliesM E Gallardo, J Lopez-Rios, I Fernaud-Espinosa, et al.
Pageof 73