Clinical and Molecular Profiles of a Cohort of Egyptian Patients with Collagen VI-Related Dystrophy by Sharaf-Eldin, Wessam E., Rafat, Karima, Issa, Mahmoud Y., Elbendary, Hasnaa M., Eissa, Noura R., Hawaary, Bahaa, Gaboon, Nagwa E. A., Maroofian, Reza, Gleeson, Joseph G., Essawi, Mona L., Zaki, Maha S.

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A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family by Gaboon, Nagwa E A, Parveen, Asia, El Beheiry, Ahmed, Al-Aama, Jumana Y, Alsaedi, Mosab S, Wasif, Naveed

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Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia by A. Gaboon, Nagwa E., Bakur, Khadijah H., Edrees, Alaa Y., Al-Aama, Jumana Y.

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Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects by Gaboon, Nagwa E.A., Banaganapalli, Babajan, Nasser, Khalidah, Razeeth, Mohammed, Alsaedi, Mosab S., Rashidi, Omran M., Abdelwehab, Lereen S., Alahmadi, Turki Saad, Safdar, Osama Y., Shaik, Jilani, Choudhry, Hani M.Z., Al-numan, Huda Husain, Khan, Mohammad Imran, Al-Aama, Jumana Y., Elango, Ramu, Shaik, Noor A.

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A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients by Gaboon, Nagwa E. A., Parveen, Asia, Ahmad, Khaled A., Shuaib, Taghreed, Al-Aama, Jumana Y., Abdelwehab, Lereen, Arif, Amina, Wasif, Naveed

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Case of Sjögren-Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis by Gaboon, Nagwa E. A., Jelani, Musharraf, Almramhi, Mona M., Mohamoud, Hussein S. A., Al-Aama, Jumana Y.

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Erratum: Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia by Gaboon, Nagwa E. A., Bakur, Khadijah H., Edrees, Alaa Y., Al-Aama, Jumana Y.

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Nutritional genomics and personalized diet by Gaboon, Nagwa E.A.

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Hereditary periodic fever syndromes by Shawky, Rabah M., Gaboon, Nagwa E.A.

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A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients by Gaboon, Nagwa E A, Parveen, Asia, Ahmad, Khaled A, Shuaib, Taghreed, Al-Aama, Jumana Y, Abdelwehab, Lereen, Arif, Amina, Wasif, Naveed

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A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family by Gaboon, Nagwa E A, Parveen, Asia, El Beheiry, Ahmed, Al-Aama, Jumana Y, Alsaedi, Mosab S, Wasif, Naveed

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Deleterious Variants in WNT10A , EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations by Parveen, Asia, Khan, Sher Alam, Mirza, Muhammad Usman, Bashir, Hina, Arshad, Fatima, Iqbal, Maria, Ahmad, Waseem, Wahab, Ahsan, Fiaz, Amal, Naz, Sidra, Ashraf, Fareeha, Mobeen, Tayyaba, Aziz, Salman, Ahmed, Syed Shoaib, Muhammad, Noor, Hassib, Nehal F, Mostafa, Mostafa I, Gaboon, Nagwa E, Gul, Roquyya, Khan, Saadullah, Froeyen, Matheus, Shoaib, Muhammad, Wasif, Naveed

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