Prenatal diagnosis of a de novo 15q11.2 microdeletion in a maternal inv(4)(p15q31) fetus with increased nuchal translucency
Author:
Funder
The Finance Department Health Special Project of Jilin Province
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference24 articles.
1. Clinical phenotypes and copy number various in children with microdeletion and microduplication syndromes: an analysis of 50 cases;Zhang;Zhongguo Dang Dai Er Ke Za Zhi,2016
2. Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray;Fan;Mol Cytogenet,2013
3. Chromosomal microarrays for the prenatal detection of microdeletions and microduplications;Wou;Clin Lab Med,2016
4. Prenatal diagnosis by chromosomal microarray analysis;Levy;Fertil Steril,2018
5. New microdeletion and microduplication syndromes: a comprehensive review;Nevado;Genet Mol Biol,2014
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