Clinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference33 articles.
1. Prenatal diagnosis of a fetus with ring chromosomal 15 by two-and three-dimensional ultrasonography;Britto;Case Rep Obstet Gynecol,2014
2. Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene;Szabó;Am J Med Genet A,2018
3. Ring chromosome 15-cytogenetics and mapping arrays: a case report and review of the literature;Paz-Y-Miño;J Med Case Rep,2018
4. Cutis tricolor parvimaculata in ring chromosome 15 syndrome: a case report;Ribeiro Dias Barroso;Pediatr Dermatol,2018
5. Prenatal diagnosis of mosaic ring chromosome 15 with abnormal maternal serum Down syndrome screening and Dandy-Walker malformation;Tan;Taiwan J Obstet Gynecol,2012
Cited by 4 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 Ring Chromosome [r(15)]: Cytogenetic Abnormality in TP53-Mutated De Novo AML-M4 Masked as Gastrointestinal Bleed With Rapidly Progressing Hyperleukocytosis and Leukostasis;Cureus;2023-09-28
2. 15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature;American Journal of Medical Genetics Part A;2023-07-12
3. Rare pathology derived from a ring chromosome 15. Clinical, genomic and protein interactome of genes associated with the phenotype;Bionatura;2022-02-15
4. The phenotype and rhGH treatment response of ring Chromosome 15 Syndrome: Case report and literature review;Molecular Genetics & Genomic Medicine;2021-11-08
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