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Barbara D'haene

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

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Methods (San Diego, Calif.)|January 12, 2010
Accurate and objective copy number profiling using real-time quantitative PCRBarbara D'haene, Jo Vandesompele, Jan Hellemans
Methods in Molecular Biology (Clifton, N.J.)|December 7, 2011
miRNA expression profiling: from reference genes to global mean normalizationBarbara D'haene, Pieter Mestdagh, Jan Hellemans, et al.
Acta Ophthalmologica|September 22, 2009
Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203Ruth Riise, Barbara D'haene, Elfride De Baere, et al.
Plos Genetics|March 22, 2013
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domainHannah Verdin, Barbara D'haene, Diane Beysen, et al.
Plos One|January 26, 2010
Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G)Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Structural and numerical changes of chromosome X in patients with esophageal atresiaErwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2010
Improved molecular diagnostics of idiopathic short stature and allied disorders: quantitative polymerase chain reaction-based copy number profiling of SHOX and pseudoautosomal region 1Barbara D'haene, Jan Hellemans, Margarita Craen, et al.
Human Genetics|October 28, 2008
Identification of copy number variants associated with BPES-like phenotypesAntoinet C J Gijsbers, Barbara D'haene, Yvonne Hilhorst-Hofstee, et al.
Plos Genetics|June 23, 2009
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screeningBarbara D'haene, Catia Attanasio, Diane Beysen, et al.
Investigative Ophthalmology & Visual Science|October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformationsBarbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Pageof 1

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

Sort By:
Pageof 1
Methods (San Diego, Calif.)|January 12, 2010
Accurate and objective copy number profiling using real-time quantitative PCRBarbara D'haene, Jo Vandesompele, Jan Hellemans
Methods in Molecular Biology (Clifton, N.J.)|December 7, 2011
miRNA expression profiling: from reference genes to global mean normalizationBarbara D'haene, Pieter Mestdagh, Jan Hellemans, et al.
Acta Ophthalmologica|September 22, 2009
Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203Ruth Riise, Barbara D'haene, Elfride De Baere, et al.
Plos Genetics|March 22, 2013
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domainHannah Verdin, Barbara D'haene, Diane Beysen, et al.
Plos One|January 26, 2010
Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G)Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Structural and numerical changes of chromosome X in patients with esophageal atresiaErwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2010
Improved molecular diagnostics of idiopathic short stature and allied disorders: quantitative polymerase chain reaction-based copy number profiling of SHOX and pseudoautosomal region 1Barbara D'haene, Jan Hellemans, Margarita Craen, et al.
Human Genetics|October 28, 2008
Identification of copy number variants associated with BPES-like phenotypesAntoinet C J Gijsbers, Barbara D'haene, Yvonne Hilhorst-Hofstee, et al.
Plos Genetics|June 23, 2009
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screeningBarbara D'haene, Catia Attanasio, Diane Beysen, et al.
Investigative Ophthalmology & Visual Science|October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformationsBarbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Pageof 1