Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients-Reference-Cited by-同舟云学术

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Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients

Published:2010-10-23 Issue:1 Volume:48 Page:1-9
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Conlin L. K.,Kramer W.,Hutchinson A. L.,Li X.,Riethman H.,Hakonarson H.,Mulley J. C.,Scheffer I. E.,Berkovic S. F.,Hosain S. A.,Spinner N. B.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 51 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. Seeing Clowns with a Ring 20 Chromosome;Archives Of Epilepsy;2024-03-01

2. Discovery of a Novel Shared Variant Among RTEL1 Gene and RTEL1-TNFRSF6B lncRNA at Chromosome 20q13.33 in Familial Progressive Myoclonus Epilepsy;International Journal of Genomics;2024-01

3. Ring Chromosome 20;Human Ring Chromosomes;2024

4. Chromosomal Abnormalities of Interest in Turner Syndrome: An Update;Journal of Pediatric Genetics;2023-07-21

5. Rare. The importance of research, analysis, reporting and education in ‘solving’ the genetic epilepsies: A perspective from the European patient advocacy group for EpiCARE;European Journal of Medical Genetics;2023-03

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