March 1997-4 Year Old Girl with Ring Chromosome 22 and Brain Tumor
Author:
Publisher
Wiley
Subject
Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1750-3639.1997.tb00902.x/fullpdf
Reference8 articles.
1. Phenotypic correlations in patients with ring chromosome 22
2. Monosomy 22 in rhabdoid or atypical tumors of the brain
3. The t(II; 22)(pI5.5; qII.23) in a retroperitoneal rhabdoid tumor also includes a regional deletion distal to CRYBB2 on 22q
4. Characterization of a new member of the human /-adaptin gene family from chromosome 22q12, a candidate meningioma gene
5. Multifocal meningiomas in a patient with a constitutional ring chromosome 22.
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1. Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22;European Journal of Medical Genetics;2023-07
2. Whole-genome sequencing analysis of an atypical teratoid/rhabdoid tumor in a patient with Phelan–McDermid syndrome: a case report and systematic review;Brain Tumor Pathology;2022-06-24
3. Case Report: The Emerging Role of Ring Chromosome 22 in Phelan-McDermid Syndrome With Atypical Teratoid/Rhabdoid Tumor: The First Child Treated With Growth Hormone;Frontiers in Neurology;2021-10-29
4. Rhabdoid Tumors;The Hereditary Basis of Childhood Cancer;2021
5. Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22;American Journal of Medical Genetics Part A;2016-10-12
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