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Chromosome 22q11 deletion and pachygyria characterized by array‐based comparative genomic hybridization

2004; Wiley; Volume: 131A; Issue: 3 Linguagem: Inglês

10.1002/ajmg.a.30377

1552-4833

David A. Koolen, Joris A. Veltman, W.O. Renier, R. Droog, Ad Geurts van Kessel, Bert B.A. de Vries,

Chromosomal and Genetic Variations

American Journal of Medical Genetics Part AVolume 131A, Issue 3 p. 322-324 Research Letter Chromosome 22q11 deletion and pachygyria characterized by array-based comparative genomic hybridization David A. Koolen, David A. Koolen Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorJoris A. Veltman, Joris A. Veltman Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorWilly O. Renier, Willy O. Renier Department of Neurology, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorRichard P. Droog, Richard P. Droog Department of Pediatrics, Elkerliek Hospital, Helmond, The NetherlandsSearch for more papers by this authorAd Geurts van Kessel, Ad Geurts van Kessel Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorBert B.A. de Vries, Corresponding Author Bert B.A. de Vries [email protected] Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsDepartment of Human Genetics, 417, University Medical Centre Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.Search for more papers by this author David A. Koolen, David A. Koolen Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorJoris A. Veltman, Joris A. Veltman Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorWilly O. Renier, Willy O. Renier Department of Neurology, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorRichard P. Droog, Richard P. Droog Department of Pediatrics, Elkerliek Hospital, Helmond, The NetherlandsSearch for more papers by this authorAd Geurts van Kessel, Ad Geurts van Kessel Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorBert B.A. de Vries, Corresponding Author Bert B.A. de Vries [email protected] Department of Human Genetics, University Medical Centre Nijmegen, Nijmegen, The NetherlandsDepartment of Human Genetics, 417, University Medical Centre Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.Search for more papers by this author First published: 02 November 2004 https://doi.org/10.1002/ajmg.a.30377Citations: 14Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Citing Literature Volume131A, Issue315 December 2004Pages 322-324 RelatedInformation