R. van Luijk

Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome.

H. Meijers-Heijboer, F. Visscher, E. van Drunen, 2001, American journal of medical genetics.

The molecular basis of the folate-sensitive fragile site FRA11A at 11q13

J. Tolmie, D. Fitzpatrick, B. Winnepenninckx, 2007, Cytogenetic and Genome Research.

Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype

R. Kooy, E. Reyniers, Y. van Bever, 2005, American journal of medical genetics. Part A.

A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.

B. Ceulemans, W. Wuyts, F. Kooy, 2006, European journal of medical genetics.

FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage

B. Kerem, D. Fitzpatrick, B. Winnepenninckx, 2007, Journal of Medical Genetics.

Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics

B. Ceulemans, J. van den Ende, F. Eyskens, 2005, Clinical genetics.

Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation.

R. Kooy, E. Reyniers, J. Wauters, 2004, Annales de genetique.

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

W. Wuyts, F. Kooy, E. Reyniers, 2007, Clinical dysmorphology.