Glass syndrome derived from chromosomal breakage downstream region of SATB2-Reference-Cited by-同舟云学术

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Glass syndrome derived from chromosomal breakage downstream region of SATB2

Published:2024-10 Issue:9 Volume:46 Page:281-285
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Shimojima Yamamoto Keiko,Shimomura Rina,Shoji Hiromichi^ORCID,Yamamoto Toshiyuki

Publisher

Elsevier BV

Reference31 articles.

1. Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase;Glass;J Med Genet,1989

2. Case series: 2q33.1 microdeletion syndrome–further delineation of the phenotype;Balasubramanian;J Med Genet,2011

3. Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome;Rifai;Am J Med Genet A,2010

4. Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome;Rosenfeld;PLoS One,2009

5. 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate;Urquhart;Eur J Med Genet,2009

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