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International Journal of Rheumatic Diseases
|
July 15, 2016
Meta-analyses of the association of HLA-DRB1 alleles with rheumatoid arthritis among Arabs
Sami Bizzari, Pratibha Nair, Mahmoud Taleb Al Ali, et al.
European Journal of Medical Genetics
|
January 29, 2019
Expanded PCH1D phenotype linked to EXOSC9 mutation
Sami Bizzari, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
Journal of Translational Medicine
|
April 21, 2016
Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference
Pratibha Nair, Sami Bizzari, Nirmal Rajah, et al.
Genes
|
October 23, 2021
Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders
Sami Bizzari, Pratibha Nair, Asha Deepthi, et al.
Journal of Pediatric Genetics
|
August 14, 2019
The Lebanese Allele in the <i>PET100</i> Gene: Report on Two New Families with Cytochrome c Oxidase Deficiency
Hicham Mansour, Sandra Sabbagh, Sami Bizzari, et al.
Molecular Syndromology
|
December 18, 2025
Blended Phenotypes in Siblings: Dual Diagnoses of Nicolaides-Baraitser and Craniosynostosis Syndromes
Sami Bizzari, Cybel Mehawej, Eliane Chouery, et al.
Frontiers in Genetics
|
May 22, 2023
Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database
Sami Bizzari, Pratibha Nair, Sayeeda Hana, et al.
European Journal of Medical Genetics
|
November 14, 2018
A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22)
André Mégarbané, Ghassan Hmaimess, Sami Bizzari, et al.
International Journal of Dermatology
|
February 26, 2017
Summary of mutations underlying autosomal recessive congenital ichthyoses (ARCI) in Arabs with four novel mutations in ARCI-related genes from the United Arab Emirates
Fatma Bastaki, Madiha Mohamed, Pratibha Nair, et al.
European Journal of Medical Genetics
|
February 2, 2020
Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3
Sami Bizzari, Lara El-Bazzal, Pratibha Nair, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
International Journal of Rheumatic Diseases
|
July 15, 2016
Meta-analyses of the association of HLA-DRB1 alleles with rheumatoid arthritis among Arabs
Sami Bizzari, Pratibha Nair, Mahmoud Taleb Al Ali, et al.
European Journal of Medical Genetics
|
January 29, 2019
Expanded PCH1D phenotype linked to EXOSC9 mutation
Sami Bizzari, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
Journal of Translational Medicine
|
April 21, 2016
Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference
Pratibha Nair, Sami Bizzari, Nirmal Rajah, et al.
Genes
|
October 23, 2021
Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders
Sami Bizzari, Pratibha Nair, Asha Deepthi, et al.
Journal of Pediatric Genetics
|
August 14, 2019
The Lebanese Allele in the <i>PET100</i> Gene: Report on Two New Families with Cytochrome c Oxidase Deficiency
Hicham Mansour, Sandra Sabbagh, Sami Bizzari, et al.
Molecular Syndromology
|
December 18, 2025
Blended Phenotypes in Siblings: Dual Diagnoses of Nicolaides-Baraitser and Craniosynostosis Syndromes
Sami Bizzari, Cybel Mehawej, Eliane Chouery, et al.
Frontiers in Genetics
|
May 22, 2023
Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database
Sami Bizzari, Pratibha Nair, Sayeeda Hana, et al.
European Journal of Medical Genetics
|
November 14, 2018
A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22)
André Mégarbané, Ghassan Hmaimess, Sami Bizzari, et al.
International Journal of Dermatology
|
February 26, 2017
Summary of mutations underlying autosomal recessive congenital ichthyoses (ARCI) in Arabs with four novel mutations in ARCI-related genes from the United Arab Emirates
Fatma Bastaki, Madiha Mohamed, Pratibha Nair, et al.
European Journal of Medical Genetics
|
February 2, 2020
Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3
Sami Bizzari, Lara El-Bazzal, Pratibha Nair, et al.
Page
of 2