Atypical teratoid rhabdoid brain tumor in an infant with ring chromosome 22
Author:
Affiliation:
1. Green Cross Genome, Seoul, Korea.
2. Department of Pathology, Catholic University of Daegu School of Medicine, Daegu, Korea.
3. Department of Pediatrics, Catholic University of Daegu School of Medicine, Daegu, Korea.
Publisher
Korean Pediatric Society
Subject
Pediatrics,Pediatrics, Perinatology, and Child Health
Link
http://kjp.or.kr/upload/pdf/kjped-57-333.pdf
Reference15 articles.
1. Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling
2. Molecular and phenotypic characterization of ring chromosome 22
3. Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations
4. Mechanisms of ring chromosome formation, ring instability and clinical consequences
5. Constitutional ring chromosomes and tumour suppressor genes.
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