A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Biochemistry
Link
http://www.nature.com/articles/hgv20168.pdf
Reference15 articles.
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2. Vera-Carbonell A, Lopez-Gonzalez V, Bafalliu JA, Ballesta-Martinez MJ, Fernandez A, Guillen-Navarro E et al. Clinical comparison of 10q26 overlapping deletions: delineating the critical region for urogenital anomalies. Am J Med Genet A 2015; 167A: 786–790.
3. Plaisancie J, Bouneau L, Cances C, Garnier C, Benesteau J, Leonard S et al. Distal 10q monosomy: new evidence for a neurobehavioral condition? Eur J Med Genet 2014; 57: 47–53.
4. Irving M, Hanson H, Turnpenny P, Brewer C, Ogilvie CM, Davies A et al. Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases. Am J Med Genet A 2003; 123A: 153–163.
5. Yatsenko SA, Kruer MC, Bader PI, Corzo D, Schuette J, Keegan CE et al. Identification of critical regions for clinical features of distal 10q deletion syndrome. Clin Genet 2009; 76: 54–62.
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