Syndromes Hidden within the 16p11.2 Deletion Region
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics
Reference39 articles.
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2. Bachmann-Gagescu R, Mefford HC, Cowan C, Glew GM, Hing AV, et al: Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. Genet Med 12:641-647 (2010).
3. Bailey JA, Eichler EE: Primate segmental duplications: crucibles of evolution, diversity and disease. Nat Rev Genet 7:552-564 (2006).
4. Ballif BC, Rosenfeld JA, Traylor R, Theisen A, Bader PI, et al: High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44. Hum Genet 131:145-156 (2012).
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