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Paper Details

Using comprehensive genomic and functional analyses for resolving genotype-phenotype mismatches in children with suspected CMMRD in Lebanon: an IRRDC study.
Hum Genet
1
2023
CMMRD, Constitutional mismatch repair deficiency, cancer, cancer predisposition syndrome, children, neurofibromatosis, patients
Author NameAffiliation
Nada JabadoMcGill University Heath Centre
Nada JabadoMcGill University Heath Centre
Cynthia HawkinsThe Hospital for Sick Children, University of Toronto, University Avenue
Cynthia HawkinsThe Hospital for Sick Children, University of Toronto, University Avenue
Uri TaboriThe Hospital for Sick Children, University of Toronto, University Avenue
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Release 1.2