Rima Korban
Jbail, JL, Lebanon
Last Updated: 09/26/2026
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Found 10 publications
Recurrent nonsense p.Trp3416* variant in the DMD gene identified in healthy Lebanese individuals: Implications for variant classification and genotype-phenotype correlations.
Journal: Journal of neuromuscular diseases
Published: August 20, 2025
Co-Occurrence of Variants in 3 Genes in a Patient with Congenital Skeletal Dysplasia and Cardiac Anomalies: Diagnostic Challenge Posed by a Blended Phenotype.
Journal: Molecular syndromology
Published: September 13, 2024
Endophilin A2 Deficiency Impairs Antibody Production in Humans.
Journal: Journal of clinical immunology
Published: August 13, 2024
Predicting Consanguinity Rates from Exome Sequencing Data in the Lebanese Population.
Journal: The Journal of molecular diagnostics : JMD
Published: August 06, 2024
POLD3 haploinsufficiency is linked to non-syndromic sensorineural adult-onset progressive hearing and balance impairments.
Journal: European journal of human genetics : EJHG
Published: April 23, 2024
Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome.
Journal: Leukemia research reports
Published: June 28, 2021
Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes.
Journal: Journal of pediatric hematology/oncology
Published: April 12, 2020
A rare case of acute myeloid leukemia with t(12;19)(q13;q13).
Journal: Leukemia research reports
Published: December 26, 2019
Untreated chronic lymphocytic leukemia in Lebanese patients: an observational study using standard karyotyping and FISH.
Journal: International journal of hematologic oncology
Published: June 12, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026