1. A rare case of acute myeloid leukemia with t(12;19)(q13;q13). (2020) Authors: Chebly, Alain; Haddad, Fady Gh; Bassil, Josiane; Yammine, Tony; Korban, Rima; Semaan, Warde; El Karak, Fady; Kourie, Hampig Raphael; Farra, Chantal Journal: Leukemia research reports Issue: Volume 14(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Abdominal Wall Desmoid during Pregnancy: Diagnostic Challenges. (3rd January 2012) Authors: Awwad, Johnny; Hammoud, Nadine; Farra, Chantal; Fares, Farah; Abi Saad, George; Ghazeeri, Ghina Other Names: Salhan S. Academic Editor.; Vaisbuch E. Academic Editor. Journal: Case reports in obstetrics and gynecology Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropenia. (3rd October 2019) Authors: Farra, Chantal; Raimondi, Susana; Abboud, Miguel Journal: Pediatric hematology and oncology Issue: Volume 36:Number 7(2019) Page Start: 432 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Alpha thalassemia allelic frequency in Lebanon. Issue 1 (4th October 2014) Authors: Farra, Chantal; Badra, Rebecca; Fares, Farah; Muwakkit, Samar; Dbaibo, Ghassan; Dabbous, Ibrahim; Ashkar, Hanine; Mounsef, Carla; Abboud, Miguel R. Journal: Pediatric blood & cancer Issue: Volume 62:Issue 1(2015:Jan.) Page Start: 120 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An unusual case of chronic lymphocytic leukemia with trisomy 12 and t(14;18) and a favorable response to ibrutinib. (2021) Authors: Haddad, Fady Gh; Chebly, Alain; El Sett, Antoine; Kourie, Hampig Raphael; Farra, Chantal Journal: Leukemia research reports Issue: Volume 15(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Analysis of ASS1 gene in ten unrelated middle eastern families with citrullinemia type 1 identifies rare and novel variants. Issue 2 (20th January 2023) Authors: Daou, Melissa; Souaid, Mirna; Yammine, Tony; Khneisser, Issam; Mansour, Hicham; Salem, Nabiha; Nemr, Antony; Awwad, Johnny; Moukarzel, Adib; Farra, Chantal Journal: Molecular genetics & genomic medicine Issue: Volume 11:Issue 2(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population. (9th December 2021) Authors: Farra, Chantal; Awwad, Johnny; Hamadeh, Lama; Khoueiry, Pierre; Halawi, Zeina; Yazbeck, Nadine; Daher, Rose; Souaid, Mirna; Hamdar, Layal; Yammine, Tony; Yunis, Khalid Journal: Annals of human genetics Issue: Volume 86:Number 2(2022) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Chloroquine and the potential adverse outcome in undiagnosed G6PD-deficient cases infected with COVID-19. (March 2021) Authors: Khneisser, Issam; Farra, Chantal Journal: Journal of medical screening Issue: Volume 28:Number 1(2021) Page Start: 54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations. Issue 6 (23rd April 2013) Authors: Caparrós‐Martin, José A.; Valencia, María; Pulido, Veronica; Martínez‐Glez, Victor; Rueda‐Arenas, Inmaculada; Amr, Khalda; Farra, Chantal; Lapunzina, Pablo; Ruiz‐Perez, Victor L.; Temtamy, Samia; Aglan, Mona Journal: American journal of medical genetics Issue: Volume 161:Issue 6(2013:Jun.) Page Start: 1354 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Ellis-van Creveld Syndrome: Mutations Uncovered in Lebanese Families. (30th April 2015) Authors: Valencia, Maria; Tabet, Lara; Yazbeck, Nadine; Araj, Alia; Ruiz-Perez, Victor L.; Charaffedine, Khalil; Fares, Farah; Badra, Rebecca; Farra, Chantal Other Names: Cotter Philip D. Academic Editor. Journal: Case reports in genetics Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗