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المؤلفون: Rafieh Alizadeh, Maryam Balali, Masoumeh Falah, Alimohamad Asghari, Massoud Houshmand, Zohreh Bagher, Mohammad Farhadi
المصدر: Fetal and Pediatric Pathology. 39:1-12
مصطلحات موضوعية: 0301 basic medicine, 030219 obstetrics & reproductive medicine, Massive parallel sequencing, biology, medicine.diagnostic_test, business.industry, First line, General Medicine, Computational biology, 030105 genetics & heredity, DNA sequencing, Pathology and Forensic Medicine, Molecular analysis, 03 medical and health sciences, 0302 clinical medicine, Pediatrics, Perinatology and Child Health, otorhinolaryngologic diseases, biology.protein, medicine, business, Gene, GJB6, Genetic testing, Heterogeneous disorder
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::1a0cd01daeb704736860a456cccbc13eTest
https://doi.org/10.1080/15513815.2019.1627625Test -
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المؤلفون: Majid Mojarrad, Javad Chezgi, Maliheh Alimardani, Atieh Eslahi, Mashsa Farjami, Mahmoud Shekari Khaniani, Sima Mansoori Derakhshan, Mohsen Rajati Haghi, Seyed Mojtaba Hosseini
المصدر: Fetal and Pediatric Pathology. 38:93-102
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Hearing loss, DNA Mutational Analysis, Cadherin Related Proteins, Nerve Tissue Proteins, Deafness, Iran, 030105 genetics & heredity, Pathology and Forensic Medicine, Iranian population, Young Adult, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, CDH23, Gene Frequency, otorhinolaryngologic diseases, Humans, Medicine, Child, Hearing Loss, Gene, Genetics, Sanger sequencing, 030219 obstetrics & reproductive medicine, Targeted mutation analysis, Myosin Heavy Chains, biology, business.industry, Genetic variants, Infant, General Medicine, Cadherins, Sulfate Transporters, Child, Preschool, Mutation, Pediatrics, Perinatology and Child Health, biology.protein, symbols, Female, medicine.symptom, business, GJB6
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10b312c9b6e0882c3220528a4ad6e58eTest
https://doi.org/10.1080/15513815.2018.1547336Test -
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المؤلفون: Marianna Mucia, Enrico Martines, Federico Sireci, Eleonora La Mattina, Francesco Martines, Pietro Salvago, P Sammarco
المساهمون: Salvago, P, Martines, E, La Mattina, E, Mucia, M, Sammarco, P, Sireci, F, Martines, F
المصدر: International Journal of Audiology. 53:558-563
مصطلحات موضوعية: Adult, Proband, Linguistics and Language, medicine.medical_specialty, Adolescent, Genotype, Hearing Loss, Sensorineural, Audiology, Connexins, Language and Linguistics, Young Adult, Speech and Hearing, Exon, Basal (phylogenetics), otorhinolaryngologic diseases, Humans, Medicine, Allele, Child, Sicily, Aged, Retrospective Studies, biology, business.industry, Sensorineural hearing loss, GJB2, Genotype-Phenotype, Middle Aged, medicine.disease, Settore MED/32 - Audiologia, Connexin 26, Settore MED/31 - Otorinolaringoiatria, Phenotype, Settore MED/03 - Genetica Medica, Sensorineural hearing lo, Mutation, Cohort, biology.protein, business, GJB6
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::076a8c7be3ba4ea66349dcca4ebf3c5dTest
https://doi.org/10.3109/14992027.2014.905717Test -
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المؤلفون: Mohammad Ali Dowlati, Javad Tavakkoly Bazzaz, Mohammad Farhadi, Massoud Houshmand, Azadeh Shojaei, Pupak Derakhshandeh-Peykar
المصدر: Mitochondrial DNA. 24:132-136
مصطلحات موضوعية: Male, Mitochondrial DNA, Biology, medicine.disease_cause, DNA, Mitochondrial, Connexins, RNA, Transfer, Phe, otorhinolaryngologic diseases, Genetics, medicine, Humans, Nucleotide, Child, Hearing Loss, Molecular Biology, Gene, chemistry.chemical_classification, Mutation, Transition (genetics), Heteroplasmy, Connexin 26, chemistry, Transfer RNA, biology.protein, GJB6
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8796ced03481458737cf2b0f942fdfdfTest
https://doi.org/10.3109/19401736.2012.717935Test -
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المؤلفون: Lilian Kimura, Regina Célia Mingroni-Netto, Ana Carla Batissoco, Luiz Artur Costa Ricardo, Maria Teresa B. M. Auricchio, Ronaldo Serafim Abreu-Silva, Ary Papa Sguillar, Daniel Rincon, Paulo Alberto Otto, Andrea R. V. R. Horimoto
المصدر: Annals of Human Biology. 38:210-218
مصطلحات موضوعية: Adult, Male, Aging, Candidate gene, medicine.medical_specialty, Genotype, Physiology, Epidemiology, Hearing loss, Biology, Audiology, Polymorphism, Single Nucleotide, Connexins, Gene Frequency, Connexin 30, otorhinolaryngologic diseases, Genetics, medicine, Genetic predisposition, Humans, SNP, Genetic Predisposition to Disease, Allele, Hearing Loss, Genetic Association Studies, Glutathione Transferase, Base Sequence, Public Health, Environmental and Occupational Health, Sequence Analysis, DNA, Middle Aged, medicine.disease, Mitochondria, Connexin 26, Haplotypes, Hearing Loss, Noise-Induced, biology.protein, Female, medicine.symptom, Brazil, Noise-induced hearing loss, GJB6
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53ee358d49c7f19af28bed3614d51a55Test
https://doi.org/10.3109/03014460.2010.513774Test -
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المؤلفون: Geir Siem, Sten Harris, Toril Fagerheim, Christoffer Jonsrud, Erik Teig, Ketil Heimdal, Andreas Früh, Claude Laurent, Trond P. Leren
المصدر: International Journal of Audiology. 49:596-605
مصطلحات موضوعية: Male, Proband, Linguistics and Language, medicine.medical_specialty, Adolescent, medicine.medical_treatment, Genetic counseling, DNA Mutational Analysis, Norwegian, Audiology, DNA, Mitochondrial, Severity of Illness Index, Connexins, Language and Linguistics, Young Adult, Speech and Hearing, Cochlear implant, Prevalence, otorhinolaryngologic diseases, medicine, Humans, Profound hearing impairment, Child, Hearing Loss, Cochlear implantation, biology, Norway, business.industry, Infant, language.human_language, Connexin 26, Cochlear Implants, Otorhinolaryngology, Child, Preschool, Mutation, language, biology.protein, Female, business, GJB6
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7fa940979cfabca1c260f3bec6e7d6bTest
https://doi.org/10.3109/14992021003743269Test -
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المؤلفون: Norma Pallares, Agustina Béhèran, Ana Belén Elgoyhen, Marcela Lipovsek, Vanesa Lotersztein, Vicente Diamante, Maria Elena Mondino, Fernando Diamante, Viviana Dalamon
المصدر: Acta Oto-Laryngologica. 129:395-398
مصطلحات موضوعية: Male, medicine.medical_specialty, Speech perception, Hearing loss, Unknown aetiology, medicine.medical_treatment, DNA Mutational Analysis, Deafness, Audiology, Connexins, Cochlear implant, Connexin 30, otorhinolaryngologic diseases, medicine, Humans, Cochlear implantation, Cochlea, biology, business.industry, Infant, General Medicine, Cochlear Implantation, Connexin 26, Otorhinolaryngology, Case-Control Studies, Child, Preschool, Mutation, Speech Perception, biology.protein, Female, sense organs, medicine.symptom, Audiometry, Speech, business, GJB6
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b01b896dc3e932ed933957f4c319805Test
https://doi.org/10.1080/00016480802566295Test