Using comprehensive genomic and functional analyses for resolving genotype-phenotype mismatches in children with suspected CMMRD in Lebanon: an IRRDC study.
Hamideh D, Das A, Bianchi V, Chung J, Negm L, Levine A, Basbous M, Sanchez-Ramirez S, Mikael L, Jabado N, Atweh L, Lteif M, Mahfouz R, Tarek N, Abboud M, Muwakkit S, Hawkins C, Tabori U, Saab R; International Replication Repair Deficiency Consortium (IRRDC).
Hamideh D, et al. Among authors: tarek n.
Hum Genet. 2023 Apr;142(4):563-576. doi: 10.1007/s00439-023-02530-8. Epub 2023 Feb 15.
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PMID: 36790526