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1دورية أكاديمية
المؤلفون: Moalla, Mariam, Hadj Kacem, Faten, Al-Mutery, Abdullah Fahad, Mahfood, Mona, Mejdoub-Rekik, Nabila, Abid, Mohamed, Mnif-Feki, Mouna, Hadj Kacem, HassenAff1, Aff3
المصدر: Journal of Assisted Reproduction and Genetics: An Official Journal of the American Society for Reproductive Medicine. 36(6):1273-1280
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2دورية أكاديمية
المؤلفون: Hamby Stephen E, Thomas Nick ST, Cooper David N, Chuzhanova Nadia
المصدر: Human Genomics, Vol 5, Iss 4, Pp 241-264 (2011)
مصطلحات موضوعية: human inherited disease, stop codon, 3'-untranslated region, nonstop mutation, nonstop mRNA decay, Medicine, Genetics, QH426-470
وصف الملف: electronic resource
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3دورية أكاديمية
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4
المؤلفون: Xiuli Wang, Xufeng Du, Guolong Zhang, Minhua Shao, Zhixiu Li, Ming Li, Yong Gu
المصدر: BMC Medical Genetics
مصطلحات موضوعية: Male, 0301 basic medicine, China, medicine.medical_specialty, Adolescent, Adenosine Deaminase, DNA Mutational Analysis, 060109 Proteomics and Intermolecular Interactions (excl. Medical Proteomics), Biology, ADAR1 gene, medicine.disease_cause, 03 medical and health sciences, Adenosine deaminase, dyschromatosis symmetrica hereditaria, Asian People, ADAR1, Genetics, medicine, Humans, Coding region, Genetics(clinical), Child, Gene, Genetics (clinical), Pigmentation disorder, Genetic spectrum, Nonstop, 060408 Genomics, Mutation, Chinese patients, Cytogenetics, novel nonstop mutation, RNA-Binding Proteins, medicine.disease, Dyschromatosis symmetrica hereditaria, Human genetics, Phenotype, 030104 developmental biology, Case-Control Studies, Child, Preschool, biology.protein, Female, Pigmentation Disorders, Research Article
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::731cec2c741b7adbd9d0627283e4f93f
https://igi.indrastra.com/items/show/28273 -
5دورية أكاديمية
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6
المصدر: Human Genomics, Vol 5, Iss 4, Pp 241-264 (2011)
ResearcherID
Human Genomicsمصطلحات موضوعية: lcsh:QH426-470, Translational termination, Nonsense-mediated decay, Mutation, Missense, human inherited disease, lcsh:Medicine, Context (language use), Biology, NonStop, Open Reading Frames, Drug Discovery, Genetics, Humans, Point Mutation, stop codon, nonstop mutation, 3' Untranslated Regions, Molecular Biology, Gene, Messenger RNA, Genome, Human, lcsh:R, Genetic Diseases, Inborn, Stop codon, lcsh:Genetics, Open reading frame, 3'-untranslated region, Codon, Nonsense, Protein Biosynthesis, nonstop mRNA decay, Codon, Terminator, Molecular Medicine, Primary Research
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7دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.