Ghent University Academic Bibliography

Show Sort by

Your filters: cql: keyword exact "DUPLICATIONS"

Mark
- journalArticle
- A1
- open access
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

Roser Corominas, Xinping Yang, Guan Ning Lin, Shuli Kang, Yun Shen, Lila Ghamsari, Martin Broly, Maria Rodriguez, Stanley Tam, Shelly A Trigg, et al.

(2014) NATURE COMMUNICATIONS. 5.
Mark
Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients

Sarah Vergult (UGent) , A Jeannette M Hoogeboom, Emilia K Bijlsma, Tom Sante (UGent) , Eva Klopocki, Bram De Wilde (UGent) , Marjolijn Jongmans, Christian Thiel, Joke BGM Verheij, Antonio Perez-Aytes, et al.

(2013) GENETICS IN MEDICINE. 15(3). p.195-202
Mark
Array comparative genomic hybridization in male infertility

K Stouffs, D Vandermaelen, A Massart, Björn Menten (UGent) , Sarah Vergult (UGent) , H Tournaye and W Lissens

(2012) HUMAN REPRODUCTION. 27(3). p.921-929
Mark
The Medicago genome provides insight into the evolution of rhizobial symbioses

Nevin D Young, Frédéric Debellé, Giles ED Oldroyd, Rene Geurts, Steven B Cannon, Michael K Udvardi, Vagner A Benedito, Klaus FX Mayer, Jérôme Gouzy, Heiko Schoof, et al.

(2011) NATURE. 480(7378). p.520-524
Mark
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations

Barbara D'haene (UGent) , Françoise Meire, Ilse Claerhout (UGent) , Hester Y Kroes, Astrid Plomp, Yvonne H Arens, Thomy de Ravel, Ingele Casteels, Sarah De Jaegere (UGent) , Sally Hooghe (UGent) , et al.

(2011) INVESTIGATIVE OPHTHALMOLOGY. 52(1). p.324-333

Academic Bibliography

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients

Array comparative genomic hybridization in male infertility

The Medicago genome provides insight into the evolution of rhizobial symbioses

Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations

Contents

Support

Contact