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G Brunner

Showing results (361-370 of 727) with videos related to

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Familial Cancer|September 27, 2013
More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counselingAisha S Sie, Wendy A G van Zelst-Stams, Liesbeth Spruijt, 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.
Journal of Genetic Counseling|November 5, 2015
High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic CounselingAisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, et al.
Pediatric Neurology|August 11, 2004
Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patientsBert van der Zwaag, Harriette T F M Verzijl, Karin H Wichers, et al.
Communications Biology|July 1, 2026
Base editing-derived models of human WDR34 and WDR60 disease alleles replicate retrograde intraflagellar transport (IFT) and hedgehog signaling defectsDinu Antony, Elif Yilmaz Güleç, Anna Klawonn, et al.
Human Mutation|April 1, 2006
The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardationJeroen van Reeuwijk, Svetlana Maugenre, Christa van den Elzen, 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.
Pageof 73

Showing results (361-370 of 727) with videos related to

Sort By:
Pageof 73
Familial Cancer|September 27, 2013
More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counselingAisha S Sie, Wendy A G van Zelst-Stams, Liesbeth Spruijt, 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.
Journal of Genetic Counseling|November 5, 2015
High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic CounselingAisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, et al.
Pediatric Neurology|August 11, 2004
Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patientsBert van der Zwaag, Harriette T F M Verzijl, Karin H Wichers, et al.
Communications Biology|July 1, 2026
Base editing-derived models of human WDR34 and WDR60 disease alleles replicate retrograde intraflagellar transport (IFT) and hedgehog signaling defectsDinu Antony, Elif Yilmaz Güleç, Anna Klawonn, et al.
Human Mutation|April 1, 2006
The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardationJeroen van Reeuwijk, Svetlana Maugenre, Christa van den Elzen, 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.
Pageof 73