Using comprehensive genomic and functional analyses for resolving genotype–phenotype mismatches in children with suspected CMMRD in Lebanon: an IRRDC study
Author:
Funder
Hospital for Sick Children
Stand Up To Cancer Canada
St. Baldrick's Foundation
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00439-023-02530-8.pdf
Reference45 articles.
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3. Alphones S, Chatterjee U, Singh A et al (2021) Immunohistochemical screening for mismatch repair protein deficiency in paediatric high-grade gliomas - institutional experience and review of literature. Childs Nerv Syst 37:2521–2530. https://doi.org/10.1007/s00381-021-05229-1
4. Amayiri N, Al-Hussaini M, Swaidan M et al (2016a) Synchronous glioblastoma and medulloblastoma in a child with mismatch repair mutation. Childs Nerv Syst 32:553–557. https://doi.org/10.1007/s00381-015-2883-3
5. Amayiri N, Tabori U, Campbell B et al (2016b) High frequency of mismatch repair deficiency among pediatric high grade gliomas in Jordan. Int J Cancer 138:380–385. https://doi.org/10.1002/ijc.29724
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