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H G Brunner

Showing results (91-100 of 179) with videos related to

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British Journal of Cancer|November 23, 2006
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instabilityC M Kets, J H J M van Krieken, K M Hebeda, et al.
Genomics|April 13, 1999
Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3R Perveen, N Hart-Holden, M J Dixon, et al.
European Journal of Cancer (Oxford, England : 1990)|August 16, 2006
Numerous high-risk epithelial lesions in familial breast cancerN Hoogerbrugge, P Bult, J J Bonenkamp, et al.
Human Molecular Genetics|February 1, 1994
Aberrant splicing of the COL4A5 gene in patients with Alport syndromeH H Lemmink, L A Kluijtmans, H G Brunner, et al.
Human Reproduction (Oxford, England)|October 2, 1998
Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor geneJ H Tuerlings, M J Ligtenberg, J A Kremer, et al.
Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
Journal of Medical Genetics|December 10, 2002
Thrombocytopenia-absent radius syndrome: a clinical genetic studyK L Greenhalgh, R T Howell, A Bottani, et al.
Human Mutation|November 16, 2005
Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing lossE Kalay, A Karaguzel, R Caylan, et al.
Clinical Genetics|January 26, 2010
Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndromeJ F Mazzeu, A M Vianna-Morgante, A C V Krepischi, et al.
Pageof 18

Showing results (91-100 of 179) with videos related to

Sort By:
Pageof 18
British Journal of Cancer|November 23, 2006
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instabilityC M Kets, J H J M van Krieken, K M Hebeda, et al.
Genomics|April 13, 1999
Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3R Perveen, N Hart-Holden, M J Dixon, et al.
European Journal of Cancer (Oxford, England : 1990)|August 16, 2006
Numerous high-risk epithelial lesions in familial breast cancerN Hoogerbrugge, P Bult, J J Bonenkamp, et al.
Human Molecular Genetics|February 1, 1994
Aberrant splicing of the COL4A5 gene in patients with Alport syndromeH H Lemmink, L A Kluijtmans, H G Brunner, et al.
Human Reproduction (Oxford, England)|October 2, 1998
Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor geneJ H Tuerlings, M J Ligtenberg, J A Kremer, et al.
Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
Journal of Medical Genetics|December 10, 2002
Thrombocytopenia-absent radius syndrome: a clinical genetic studyK L Greenhalgh, R T Howell, A Bottani, et al.
Human Mutation|November 16, 2005
Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing lossE Kalay, A Karaguzel, R Caylan, et al.
Clinical Genetics|January 26, 2010
Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndromeJ F Mazzeu, A M Vianna-Morgante, A C V Krepischi, et al.
Pageof 18