Výsledky vyhledávání - Nasir Al‐Allawi
- Zobrazuji výsledky 1 - 4 z 4
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Epidemiological profile of common haemoglobinopathies in Arab countries Autor Hanan Hamamy, Nasir Al‐Allawi
Vydáno 2012Artigo -
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3
Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families Autor Periklis Makrythanasis, Mari Nelis, Federico Santoni, Michel Guipponi, Anne Vannier, Frédérique Béna, Stefania Gimelli, Elisavet Stathaki, Samia A. Temtamy, André Mégarbané, Amira Masri, Mona Aglan, Maha S. Zaki, Armand Bottani, Siv Fokstuen, Lorraine Gwanmesia, Konstantinos A. Aliferis, Mariana Bustamante Eduardo, Georgios Stamoulis, Stavroula Psoni, Sofia Kitsiou‐Tzeli, Helen Fryssira, Emmanouil Kanavakis, Nasir Al‐Allawi, Abdelaziz Sefiani, Sana' A. S. Al Hait, Siham Chafai Elalaoui, Nadine Jalkh, Lihadh Al‐Gazali, Fatma Al‐Jasmi, Habiba Chaabouni Bouhamed, Ebtesam Abdalla, D.N. Cooper, Hanan Hamamy, Stylianos E. Antonarakis
Vydáno 2014Artigo -
4
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders Autor Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki, Matan Hofree, Jennifer L. Silhavy, Andrew Heiberg, Mostafa Abdellateef, Başak Rosti, Eric Scott, Lobna Mansour, Amira Masri, Hülya Kayserili, Jumana Y. Al‐Aama, Ghada M. H. Abdel‐Salam, Ariana Karminejad, Majdi Kara, Bülent Kara, Babak Bozorgmehri, Tawfeg Ben‐Omran, Faezeh Mojahedi, Iman G. Mahmoud, Naïma Bouslam, Ahmed Bouhouche, Ali Benomar, Sylvain Hanein, Laure Raymond, Sylvie Forlani, Massimo Mascaro, Laila Selim, Nabil Shehata, Nasir Al‐Allawi, Parayil Sankaran Bindu, Matloob Azam, Murat Günel, Ahmet Okay Çağlayan, Kaya Bilgüvar, Aslıhan Tolun, Mahmoud Y. Issa, Jana Schroth, Emily Spencer, Rasim Özgür Rosti, Naiara Akizu, Keith K. Vaux, Anide Johansen, Alice A. Koh, Hisham Megahed, Alexandra Dürr, Alexis Brice, Giovanni Stévanin, Stacy Gabriel, Trey Ideker, Joseph G. Gleeson
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Disease
Gene
Medicine
Pathology
Environmental health
Exome
Exome sequencing
Genetic counseling
Genotype
Internal medicine
Phenotype
Thalassemia
Amyotrophic lateral sclerosis
Beta thalassemia
Candidate gene
Consanguinity
Corticospinal tract
Diffusion MRI
Disease gene identification
Epidemiology
Family medicine
Fetus
Genetic heterogeneity
Genetic testing
Haplotype
Hemoglobinopathy
Hereditary spastic paraplegia
Magnetic resonance imaging