Publications by authors named "Rob Van Luijk"

Claim this Profile
A
A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
Winnie Courtens, Jan Wauters, Marek Wojciechowski, Edwin Reyniers, Stefan Scheers, Rob van Luijk

Clin Dysmorphol· October 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage.
Kim Debacker, Birgitta Winnepenninckx, Neta Ben-Porat, David FitzPatrick, Rob Van Luijk

J Med Genet· May 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
Winnie Courtens, Wim Wuyts, Stefaan Scheers, Rob Van Luijk, Edwin Reyniers

Eur J Med Genet· November 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.
Liesbeth Rooms, Edwin Reyniers, Stefaan Scheers, Rob van Luijk, Jan Wauters

Eur J Hum Genet· October 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.
Arvid Suls, Kristl G Claeys, Dirk Goossens, Boris Harding, Rob Van Luijk

Hum Mutat· September 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype.
Yolande van Bever, Liesbeth Rooms, Annick Laridon, Edwin Reyniers, Rob van Luijk

Am J Med Genet A· May 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation.
Liesbeth Rooms, Edwin Reyniers, Rob van Luijk, Stefan Scheers, Jan Wauters

Ann Genet· December 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA).
Liesbeth Rooms, Edwin Reyniers, Rob van Luijk, Stefaan Scheers, Jan Wauters

Hum Mutat· January 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis