Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s004310050782.pdf
Cited by 28 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. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature;Molecular Cytogenetics;2018-02-05
2. A case of Tetrasomy 15q with left cleft lip and alveolus;Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology;2017-09
3. Avoiding a second amniocentesis to corroborate prenatal diagnosis by using refrigerated samples*;The Journal of Maternal-Fetal & Neonatal Medicine;2016-05-26
4. Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome;Journal of Neurodevelopmental Disorders;2016-05-06
5. Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases;European Journal of Medical Genetics;2014-01
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