Publications by authors named "Rob van Luijk"

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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

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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

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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

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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

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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

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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

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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

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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

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