Method for the molecular cytogenetic visualization of fragile site FRAXA
Author:
Publisher
Pleiades Publishing Ltd
Subject
Structural Biology,Biophysics
Link
http://link.springer.com/content/pdf/10.1134/S0026893317040069.pdf
Reference26 articles.
1. Martin J.P., Bell J. 1943. A pedigree of mental defect showing sex-linkage. J. Neurol. Psychiatry. 6, 154–157.
2. Saldarriaga W., Tassone F., González-Teshima L.Y., Forero-Forero J.V., Ayala-Zapata S., Hagerman R. 2014. fragile X syndrome. Colombia Médica. 45, 190–198.
3. Hunter J., Rivero-Arias O., Angelov A., Kim E., Fotheringham I., Leal J. 2014. Epidemiology of fragile X syndrome: A systematic review and meta-analysis. Am. J. Med. Genet. Part A. 164, 1648–1658.
4. D’Hulst C., Kooy R.F. 2009. Fragile X syndrome: From molecular genetics to therapy. J. Med. Genet. 46, 577–584.
5. Monaghan K.G., Lyon E., Spector E. 2013. ACMG standards and guidelines for fragile X testing: A revision to the disease-specific supplements to the standards and guidelines for clinical genetics laboratories of the American college of medical genetics and genomics. Genet. Med. 15, 575–586.
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