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H G Brunner

Showing results (101-110 of 179) with videos related to

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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.
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.
The New England Journal of Medicine|February 18, 1993
Brief report: reverse mutation in myotonic dystrophyH G Brunner, G Jansen, W Nillesen, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiencyJ W M Martens, S Lumbroso, M Verhoef-Post, 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.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
International Journal of Cancer|October 25, 2007
Is early-onset microsatellite and chromosomally stable colorectal cancer a hallmark of a genetic susceptibility syndrome?C M Kets, J H J M van Krieken, P E J van Erp, et al.
American Journal of Human Genetics|June 1, 1993
X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolismH G Brunner, M R Nelen, P van Zandvoort, et al.
Pageof 18

Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
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.
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.
The New England Journal of Medicine|February 18, 1993
Brief report: reverse mutation in myotonic dystrophyH G Brunner, G Jansen, W Nillesen, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiencyJ W M Martens, S Lumbroso, M Verhoef-Post, 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.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
International Journal of Cancer|October 25, 2007
Is early-onset microsatellite and chromosomally stable colorectal cancer a hallmark of a genetic susceptibility syndrome?C M Kets, J H J M van Krieken, P E J van Erp, et al.
American Journal of Human Genetics|June 1, 1993
X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolismH G Brunner, M R Nelen, P van Zandvoort, et al.
Pageof 18