Development of patients with 47,XX,+13/45,X mosaics: Case report and review of the literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00431-013-2001-z.pdf
Reference16 articles.
1. Baty BJ, Jorde LB, Blackburn BL, Carey JC (1994) Natural history of trisomy 18 and trisomy 13: II. Psychomotor development. Am J Med Genet 49(2):189–194. doi: 10.1002/ajmg.1320490205
2. Bondy CA (2007) Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group. J Clin Endocrinol Metab 92(1):10–25. doi: 10.1210/jc.2006-1374
3. Carey JC (2010) Trisomy 18 and trisomy 13 syndromes. In: Management of genetic syndromes. Wiley, New York, pp. 807–823. doi: 10.1002/9780470893159.ch54
4. Chen M, Yeh GP, Shih JC, Wang BT (2004) Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy. Prenat Diagn 24(2):137–143. doi: 10.1002/pd.814
5. Delatycki M, Gardner RJ (1997) Three cases of trisomy 13 mosaicism and a review of the literature. Clin Genet 51(6):403–407
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance;American Journal of Medical Genetics Part A;2018-08-06
2. A rare case of mosaic 45,X/47,XX,+13 in 28-year-old women with secondary amenorrhoea: A case report and literature review;Meta Gene;2015-02
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