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TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.
Published in:
European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1090, doi. 10.1038/sj.ejhg.5201674
By:
- Rooms, Liesbeth;
- Reyniers, Edwin;
- Scheers, Stefaan;
- van Luijk, Rob;
- Wauters, Jan;
- Van Aerschot, Leen;
- Callaerts-Vegh, Zsuzsanna;
- D'Hooge, Rudi;
- Mengus, Gabrielle;
- Davidson, Irwin;
- Courtens, Winnie;
- Kooy, R. Frank
Publication type:
Article
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.
Published in:
Human Mutation, 2006, v. 27, n. 9, p. 914, doi. 10.1002/humu.20350
By:
- Suls, Arvid;
- Claeys, Kristl G.;
- Goossens, Dirk;
- Harding, Boris;
- Luijk, Rob Van;
- Scheers, Stefaan;
- Deprez, Liesbet;
- Audenaert, Dominique;
- Dyck, Tine Van;
- Beeckmans, Sabine;
- Smouts, Iris;
- Ceulemans, Berten;
- Lagae, Lieven;
- Buyse, Gunnar;
- Barisic, Nina;
- Misson, Jean-Paul;
- Wauters, Jan;
- Del-Favero, Jurgen;
- De Jonghe, Peter;
- Claes, Lieve R.F.
Publication type:
Article
Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA) (Communicated by Ulf Landegren).
Published in:
Human Mutation, 2004, v. 23, n. 1, p. 17, doi. 10.1002/humu.10300
By:
- Liesbeth Rooms;
- Edwin Reyniers;
- Rob van Luijk;
- Stefaan Scheers;
- Jan Wauters;
- Berten Ceulemans;
- Jenneke Van Den Ende;
- Yolande Van Bever;
- R. Frank Kooy
Publication type:
Article

Found: 3

TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA) (Communicated by Ulf Landegren).