New candidate region for mirror hand movements: two patients with terminal 9p deletion and 20p duplication
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s11033-023-09192-9.pdf
Reference18 articles.
1. Hauge X, Raca G, Cooper S, May K, Spiro R, Adam M et al (2008) Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p. Genet Med 10(8):599–611. https://doi.org/10.1097/gim.0b013e31817e2bde
2. Swinkels ME, Simons A, Smeets DF, Vissers LE, Veltman JA, Pfundt R et al (2008) Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype. Am J Med Genet A 146A(11):1430–1438. https://doi.org/10.1002/ajmg.a.32310
3. Chen G, Xiong S, Zou G, Wu F, Qu X, Alawbathani S et al (2022) A 6.3 mb maternally derived microduplication of 20p13p12.2 in a fetus with brachydactyly type D and related literature review. Mol Cytogenet 15(1):6. https://doi.org/10.1186/s13039-022-00584-3
4. Sidwell RU, Pinson MP, Gibbons B, Byatt SA, Svennevik EC, Hastings RJ et al (2000) Pure trisomy 20p resulting from isochromosome formation and whole arm translocation. J Med Genet 37(6):454–458. https://doi.org/10.1136/jmg.37.6.454
5. Thomas MA, Duncan AM, Bardin C, Kaloustian VM (2004) Lissencephaly with Der(17)t(17;20)(p13.3;p12.2)mat. Am J Med Genet A 124A(3):292–295. https://doi.org/10.1002/ajmg.a.20373
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