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Hanan Abdelhalim ElSokary
Hanan Abdelhalim ElSokary
King Abdulaziz University
Phenotype
Missense mutation
Consanguinity
Exome sequencing
Zebrafish
2
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Genetic association study of NOD2 and IL23R amino acid substitution polymorphisms in saudi inflammatory bowel disease patients
2021
Journal of King Saud University - Science
Raneem Saadi Alharbi
Noor Ahmad Shaik
Hadiah Bassam AlMahdi
Hanan Abdelhalim ElSokary
Bassam Adnan Jamalalail
Mahmoud Mosli
Hadeel A. Alsufyani
Jumana Y. Al-Aama
Ramu Elango
Omar I. Saadah
Babajan Banganapalli
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Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects.
2021
Frontiers of Medicine in China
Rabab Said Alsafwani
Khalidah Khalid Nasser
Thoraia Shinawi
Babajan Banaganapalli
Hanan Abdelhalim ElSokary
Zhaher F. Zaher
Noor Ahmad Shaik
Gaser Abdelmohsen
Jumana Y. Al-Aama
Adam J. Shapiro
Osman O. Al Radi
Ramu Elango
Turki S. Alahmadi
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