De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency
Author:
Publisher
Wiley
Subject
Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-0528.2008.01948.x/fullpdf
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1. Clinical phenotype of the 16p.13.11 microdeletion: a case report with a mini review of the literature;Frontiers in Genetics;2024-08-16
2. Array study in fetuses with nuchal translucency above the 95th percentile: a 4-year observational single-centre study;Archives of Gynecology and Obstetrics;2022-04-29
3. Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches;Frontiers in Genetics;2022-03-15
4. Prenatal diagnosis of Smith–Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects;Taiwanese Journal of Obstetrics and Gynecology;2016-12
5. Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis;Ultrasound in Obstetrics & Gynecology;2015-12
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