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1دورية أكاديمية
المؤلفون: Avdjieva-Tzavella D., Mihailova S., Lukanov C., Naumova E., Simeonov E., Tincheva R., Toncheva D.
المصدر: Balkan Journal of Medical Genetics, Vol 15, Iss 2, Pp 47-53 (2012)
مصطلحات موضوعية: autism spectrum disorders (asds), genetic testing, mitochondrial dna (mtdna) mutations, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1311-0160
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2دورية أكاديمية
المصدر: Balkan Journal of Medical Genetics, Vol 15, Iss 1, Pp 25-29 (2012)
مصطلحات موضوعية: mitochondrial dna (mtdna) mutations, chronic cervicitis, cervical cancer, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1311-0160
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المؤلفون: M Kara, S Oztas, Abdulgani Tatar, Bunyamin Borekci, F Dagli
المصدر: Balkan Journal of Medical Genetics, Vol 15, Iss 1, Pp 25-29 (2012)
Balkan Journal of Medical Genetics : BJMGمصطلحات موضوعية: Cervical cancer, Pathology, medicine.medical_specialty, Mitochondrial DNA, cervical cancer, mitochondrial dna (mtdna) mutations, Chronic Cervicitis, Cancer, Cervicitis, chronic cervicitis, Biology, QH426-470, medicine.disease, Heteroplasmy, law.invention, medicine.anatomical_structure, law, Immunology, medicine, Genetics, Original Article, Cervix, Genetics (clinical), Polymerase chain reaction
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4دورية أكاديمية
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المؤلفون: Jessica A. Hellings, Merlin G. Butler, Sukhbir Dhillon
المصدر: Current Genomics
مصطلحات موضوعية: Genetics, Mitochondrial DNA, Nuclear gene, Biology, Mitochondrion, Bioinformatics, medicine.disease, nuclear genes, Autism spectrum disorders (ASD), DNA sequencing, Article, Fragile X syndrome, mitochondrial DNA (mtDNA) mutations and depletion, lactate/pyruvate ratios, mental disorders, medicine, Autism, oxidative stress, Copy-number variation, Epigenetics, Genetics (clinical), genetic causation
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09063546b220735e16e1472986ca4f26
https://pubmed.ncbi.nlm.nih.gov/22294875 -
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المؤلفون: Ingeborg Liebaers, Ann Meulemans, Linda De Meirleir, Joél Smet, Sara Seneca, Rudy Van Coster, Willy Lissens, Marie-Cécile Nassogne
المساهمون: Pediatrics, Centre for Medical Genetics, Department of Embryology and Genetics, Vrije Universiteit Brussel
المصدر: Vrije Universiteit Brussel
مصطلحات موضوعية: Male, Mitochondrial DNA, Mitochondrial disease, NADH-ubiquinone oxidoreductase, mitochondrial DNA (mtDNA) mutations, Oxidative phosphorylation, Heteroduplex Analysis, Biology, MT-RNR1, Nucleic Acid Denaturation, DNA, Mitochondrial, chemistry.chemical_compound, Mitochondrial Encephalomyopathies, medicine, Humans, Disease-causing Mutation, Age of Onset, Child, Coloring Agents, Gene, Genetics, Electron Transport Complex I, Polymorphism, Genetic, Reverse Transcriptase Polymerase Chain Reaction, complex I, Structural gene, Infant, Newborn, Infant, General Medicine, medicine.disease, Electrophoresis, Gel, Pulsed-Field, chemistry, Child, Preschool, Pediatrics, Perinatology and Child Health, Mutation, Female, Neurology (clinical), DNA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab72f3c6c6f14664af65ad870cfb94d1
https://biblio.vub.ac.be/vubir/analysis-of-the-mitochondrial -encoded-subunits-of-complex-i-in-20-patients-with-a-complex-i-deficiency(49562a64-96f0-4e14-92e6-8f12c98bcdad).html -
7دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
8دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.