The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype-Reference-Cited by-同舟云学术

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

Published:2009-10-07 Issue:2 Volume:18 Page:163-170
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

van Bon Bregje WM,Koolen David A,Brueton Louise,McMullan Dominic,Lichtenbelt Klaske D,Adès Lesley C,Peters Gregory,Gibson Kate,Novara Francesca,Pramparo Tiziano,Bernardina Bernardo Dalla,Zoccante Leonardo,Balottin Umberto,Piazza Fausta,Pecile Vanna,Gasparini Paolo,Guerci Veronica,Kets Marleen,Pfundt Rolph,de Brouwer Arjan P,Veltman Joris A,de Leeuw Nicole,Wilson Meredith,Antony Jayne,Reitano Santina,Luciano Daniela,Fichera Marco,Romano Corrado,Brunner Han G,Zuffardi Orsetta,de Vries Bert BA

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2009152.pdf

Reference27 articles.

1. Mefford HC, Sharp AJ, Baker C et al: Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. N Engl J Med 2008; 359: 1685–1699.

2. Gajecka M, Mackay KL, Shaffer LG : Monosomy 1p36 deletion syndrome. Am J Med Genet C Semin Med Genet 2007; 145C: 346–356.

3. Koolen DA, Sharp AJ, Hurst JA et al: Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. J Med Genet 2008; 45: 710–720.

4. Ben-Shachar S, Ou Z, Shaw CA et al: 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome. Am J Hum Genet 2008; 82: 214–221.

5. Ballif BC, Hornor SA, Jenkins E et al: Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2. Nat Genet 2007; 39: 1071–1073.

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