Diagnosis of distal 22q11.2 deletion syndrome in a patient with a teratoid/rhabdoid tumour
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference17 articles.
1. 22q11.2 distal deletion: a recurrent Genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome;Ben-Shachar;Am. J. Hum. Genet.,2008
2. Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumours;Biegel;Cancer Res.,1999
3. hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities;Bourdeaut;J. Pathol.,2007
4. A common molecular basis for rearrangement disorders on chromosome 22q11;Edelmann;Hum. Mol. Genet.,1999
5. High-density single nucleotide polymorphism array analysis in patients with germilne deletions of 22q11.2 and malignant rhabdoid tumour;Jackson;Hum. Genet.,2007
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