Prenatal diagnosis of partial monosomy 21q (21q22.1→qter) associated with intrauterine growth restriction and corpus callosum dysgenesis
Author:
Funder
Ministry of Science and Technology
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference7 articles.
1. Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literature;Burgess;Case Rep Genet,2014
2. Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21;Lyle;Eur J Hum Genet,2009
3. Genomic analysis of partial 21q monosomies with variable phenotypes;Roberson;Eur J Hum Genet,2011
4. Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature;Errichiello;Mol Cytogenet,2016
5. A prenatally diagnosed patient with full monosomy 21: ultrasound, cytogenetic, clinical, molecular, and necropsy findings;Mori;Am J Med Genet A,2004
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. How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review;Taiwanese Journal of Obstetrics and Gynecology;2021-11
2. De novo mosaic and partial monosomy of chromosome 21 in a case with superior vena cava duplication;Molecular Cytogenetics;2020-09-12
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