Molecular characterization of de novo ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1007/s12041-023-01439-5.pdf
Reference23 articles.
1. Bertini V., Valetto A., Uccelli A., Tarantino E. and Simi P. 2008 Ring chromosome 21 and reproductive pattern: a familial case and review of the literature. Fertil. Steril. 90, e1–e5.
2. Chen C. P., Wang L. K., Chern S. R., Wu P. S., Chen S. W., Wu F. T. et al. 2021 Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion. Taiw. J. Obstet. Gynecol. 60, 157–160.
3. Dallapiccola B., De Filippis V., Notarangelo A., Perla G. and Zelante L. 1986 Ring chromosome 21 in healthy persons: different consequences in females and males. Hum. Genet. 73, 218–220.
4. Falik-Borenstein T. C., Pribyl T. M., Pulst S. M., Van Dyke D. L., Weiss L., Chu M. L. et al. 1992 Stable ring chromosome 21: molecular and clinical definition of the lesion. Am. J. Med. Genet. 42, 22–28.
5. Guilherme R. S., Ayres Meloni V. F., Kim C. A., Pellegrino R., Takeno S. S., Spinner N. B. et al. 2011 Mechanisms of ring chromosome formation, ring instability and clinical consequences. BMC Med. Genet. 12, 171.
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