Clinical genetic description and analysis of the case of chromosomal mosaicism mos47,XY,+8/46,XY
Author:
Affiliation:
1. Kemerovo Regional Clinical Hospital named after S.V. Belyaev
2. Kemerovo Regional Clinical Hospital named after S.V. Belyaev; Kemerovo State Medical University
Publisher
Siberian State Medical University
Subject
Molecular Medicine
Reference14 articles.
1. Nicolaides K.H. Screening for fetal aneuploidies at 11 to 13 weeks. Prenat. Diagn. 2011; 31 (1): 7–15. DOI: 10.1002/pd.2637.
2. Chen C.P., Chen M., Pan Y.J., Su Y.N., Chern S.R., Tsai F.J., Chen Y.T., Wang W. Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review. Taiwanese Journal of Obstetrics & Gynecology. 2011; 50(3): 331–338. DOI: 10.1016/j.tjog.2011.07.013.
3. Paulsson K., Säll T., Fioretos T., Mitelman F., Johansson B. The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology. Cancer Genet. Cytogenet. 2001; 130 (2): 160–165. DOI: 10.1016/s0165-4608(01)
4. Becker K., FitzGerald O., Green A.J., Keogan M., Newbury-Ecob R., Greenhalgh L. Withers S., Hollox E.J., Aldred P.M.R., Armour J.A.L. Constitutional trisomy 8 and Behcet syndrome. Am. J. Med. Genet. 2009; 149A (5): 982–986. DOI: 10.1002/ajmg.a.32756.
5. Rauen K.A., Golabi M., Cotter P.D. Fertility in a female with mosaic trisomy 8. Fertility and Sterility. 2003; 79 (1): 206–208. doi: 10.1016/s0015-0282(02)04410-2.
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