Molecular and Cytogenetic Characterization of a Fetus with Mosaic Ring Chromosome 13
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference5 articles.
1. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13;Chen;Gene,2013
2. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13;Su;Genet Mol Res,2013
3. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: Clues to the mechanisms of formation;Rossi;J Med Genet,2008
4. Preliminary definition of a “critical region” of chromosome 13 in q32: Report of 14 cases with 13q deletions and review of the literature;Brown;Am J Med Genet,1993
5. Prenatal diagnosis of a partial trisomy 13q (q14→qter): Phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization;Machado;Genet Mol Res,2010
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. Ring Chromosome 13;Human Ring Chromosomes;2024
2. Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature;Taiwanese Journal of Obstetrics and Gynecology;2021-05
3. Lessons from a 30 year follow‐up of monozygotic twins with discordant phenotype due to a ring 13 chromosomal mosaicism in one of them;American Journal of Medical Genetics Part A;2021-01-13
4. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2020-01
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