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Chantal Farra

Showing results (1-10 of 60) with videos related to

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Journal of Medical Screening|May 9, 2020
Chloroquine and the potential adverse outcome in undiagnosed G6PD-deficient cases infected with COVID-19Issam Khneisser, Chantal Farra
Pediatric Hematology and Oncology|August 15, 2019
Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropeniaChantal Farra, Susana Raimondi, Miguel Abboud
Annals of Thoracic Medicine|November 10, 2017
A novel cystic fibrosis gene mutation c.2490insT in a Palestinian patient: A case report and review of the literatureHassan Chami, Samer Abou Arbid, Rebecca Badra, et al.
Fetal Diagnosis and Therapy|June 18, 2002
Congenital bowing of long bones: prenatal ultrasound findings and diagnostic dilemmasChantal Farra, Caroline Piquet, Marc Guillaume, et al.
Epilepsy & Behavior : E&B|February 24, 2009
Two new familial severe infantile spasm syndromes in malesPascale E Karam, Chantal Farra, Alhan Shamseddine, et al.
American Journal of Medical Genetics. Part A|December 14, 2006
A patient with duplication (7)(p22.1pter) characterized by array-CGHLaila Zahed, Tiziano Pramparo, Chantal Farra, et al.
Clinical Dysmorphology|February 13, 2023
Novel intronic JAG1 variant associated with Alagille syndrome in a three-generation Lebanese family with variable featuresJohnny Awwad, Tony Yammine, Layal Hamdar, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2020
DNMT3B deficiency presenting as severe combined immune deficiency: A case reportCybel Mehawej, Hassan Khalife, Rima Hanna-Wakim, et al.
BMC Medical Genetics|September 7, 2019
BRCA mutations in a cohort of Iraqi patients presenting to a tertiary referral centerChantal Farra, Christelle Dagher, Lama Hamadeh, et al.
Molecular Biology Reports|May 25, 2023
Novel SCN9A variant associated with congenital insensitivity to painTony Yammine, Raffi Aprahamian, Mirna Souaid, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Journal of Medical Screening|May 9, 2020
Chloroquine and the potential adverse outcome in undiagnosed G6PD-deficient cases infected with COVID-19Issam Khneisser, Chantal Farra
Pediatric Hematology and Oncology|August 15, 2019
Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropeniaChantal Farra, Susana Raimondi, Miguel Abboud
Annals of Thoracic Medicine|November 10, 2017
A novel cystic fibrosis gene mutation c.2490insT in a Palestinian patient: A case report and review of the literatureHassan Chami, Samer Abou Arbid, Rebecca Badra, et al.
Fetal Diagnosis and Therapy|June 18, 2002
Congenital bowing of long bones: prenatal ultrasound findings and diagnostic dilemmasChantal Farra, Caroline Piquet, Marc Guillaume, et al.
Epilepsy & Behavior : E&B|February 24, 2009
Two new familial severe infantile spasm syndromes in malesPascale E Karam, Chantal Farra, Alhan Shamseddine, et al.
American Journal of Medical Genetics. Part A|December 14, 2006
A patient with duplication (7)(p22.1pter) characterized by array-CGHLaila Zahed, Tiziano Pramparo, Chantal Farra, et al.
Clinical Dysmorphology|February 13, 2023
Novel intronic JAG1 variant associated with Alagille syndrome in a three-generation Lebanese family with variable featuresJohnny Awwad, Tony Yammine, Layal Hamdar, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2020
DNMT3B deficiency presenting as severe combined immune deficiency: A case reportCybel Mehawej, Hassan Khalife, Rima Hanna-Wakim, et al.
BMC Medical Genetics|September 7, 2019
BRCA mutations in a cohort of Iraqi patients presenting to a tertiary referral centerChantal Farra, Christelle Dagher, Lama Hamadeh, et al.
Molecular Biology Reports|May 25, 2023
Novel SCN9A variant associated with congenital insensitivity to painTony Yammine, Raffi Aprahamian, Mirna Souaid, et al.
Pageof 6