Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene von Neissi, Mostafa, Mohammadi-Asl, Javad, Mohammadi-Asl, Misagh, Roghani, Mojdeh, Sheikh-Hosseini, Motahareh, Issa Al-Badran, Adnan

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Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9 von Neissi, Mostafa, Sheikh‐Hosseini, Motahareh, Mohammadi‐Asl, Misagh, Al‐Badran, Adnan Issa, Roghani, Mojdeh, Mohammadi‐Asl, Javad, Jorfi, Kamele

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Mutational spectrum of the AP3B1 gene in an Iraqi family affected with Hermansky-Pudlak syndrome type 2 von Neissi, Mostafa, Al-Badran, Adnan Issa

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Profile of Interleukin-6 and Tumor Necrosis Factor-α in Hospitalized COVID-19 Patients von Saeed, Khlood Noori, Shnawa, Bushra Hussain, Al-Badran, Adnan Issa

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Homozygous AHI1 gene mutation (c.1213A>C; Thr405Pro) leads to Joubert syndrome in a consanguineous Iranian family: A case report von Neissi, Mostafa, Issa Al-Badran, Adnan, Mohammadi-Asl, Javad

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A novel missense mutation in PLEKHG5 gene causing an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease in an Iraqi family von Neissi, Mostafa, Mabudi, Hadideh, Al-Badran, Adnan Issa, Mohammadi-Asl, Javad, Al-Badran, Raed Abdulelah

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Exome sequencing identifies a novel GUCY2D mutation in an Iranian family with Leber congenital amaurosis-1: a case report von Neissi, Mostafa, Al-Badran, Adnan Issa, Mohammadi-Asl, Javad

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Joubert syndrome caused by a TMEM67 mutation: Genotype-phenotype analysis von Neissi, Mostafa, Misagh Mohammadi-Asl, Mojdeh Roghani, Issa Al-Badran, Adnan, Motahareh Sheikh-Hosseini, Mohammadi-Asl, Javad

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Mutation Detection in MYO15A Gene in an Iranian Family with Non-Syndromic Hearing Loss von Mostafa Neissi, Mostafa Neissi, Mohammadi-Asl, Misagh, Roghani, Mojdeh, Al-Badran, Adnan, Mohammadi-Asl, Javad

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A Novel SLC9A6 Mutation Associated with Christianson Syndrome in a Non-Consanguineous Iranian Family: A Case Report von Mehdi Hashemipour, Mostafa Neissi, Mahsa Rashid, Karim Sevari, Motahareh Sheikh-Hosseini, Adnan Issa Al-Badran

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A novel heterozygous TPM2 gene mutation in an Iranian family affected by distal arthrogryposis type 1: a case report von Neissi, Mostafa, Sheikh-Hosseini, Motahareh, Mohammadi-Asl, Javad, Al-Badran, Adnan Issa

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Clinical and genetic analysis of Niemann-Pick disease type C with a novel NPC1 variant von Neissi, Mostafa, Al-Badran, Adnan Issa, Mohammadi-Asl, Misagh, Al-Badran, Raed Abdulelah, Sheikh-Hosseini, Motahareh, Roghani, Mojdeh, Mohammadi-Asl, Javad

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Detection of an FYCO1 nonsense mutation in an affected patient with autosomal recessive cataract : a case report von Al-Badran, Raed Abdulelah, Al-Badran, Adnan Issa, Mabudi, Hadideh, Neissi, Mostafa, Mohammadi-Asl, Javad

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Hormone receptor-related gene polymorphisms and prostate cancer risk in North Indian population von Onsory, Khadijeh, Sobti, R. C, Al-Badran, Adnan Issa, Watanabe, Masatoshi, Shiraishi, Taizo, Krishan, Awtar, Mohan, Harsh, Kaur, Pushpinder

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Mitochondrial DNA (hypervariable region I) diversity in Basrah population – Iraq von Ohied, Bassim Muften, Al-Badran, Adnan Issa

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Y-chromosome variation in Basrah population von Ohied, Bassim Muften, Al-Badran, Adnan Issa

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Study some physical properties of thin films of DNA-CTMA and DNA-CTMA/PMMA von Ali, Ali S., Zaidan, Karema M., Al-Badran, Adnan Issa

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A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss von Neissi, Mostafa, Al-Badran, Adnan Issa, Mohammadi-Asl, Javad

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A study of the relationship between the Galectin-9 gene (LGALS9) in three types of cancer patients in Basrah, Iraq von Ayoob, Anwar N., Al-Badran, Adnan Issa, Abood, Rafid A.

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Preparation of Poly (methyl methacrylate) thin film Capacitors on ITO-glass substrate von S. Ali, Ali, M. Zaidan, Karema, Issa Al-Badran, Adnan

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