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المؤلفون: Mustafa Tekin, Duygu Duman, Armagan Incesulu, S Taşır-Yılmaz, Seyra Erbek, Hatice Ozturkmen-Akay, Asli Sirmaci, Hilal Özdağ
المصدر: Clinical Genetics. 75:562-567
مصطلحات موضوعية: Turkey, Hearing loss, Hearing Loss, Sensorineural, DNA Mutational Analysis, Molecular Sequence Data, Consanguinity, Biology, Compound heterozygosity, Polymorphism, Single Nucleotide, Connexins, Gene Frequency, Genetics, medicine, Humans, Point Mutation, Genetic Testing, Allele frequency, Genetics (clinical), Base Sequence, Genome, Human, Point mutation, Haplotype, Membrane Proteins, DNA, medicine.disease, Connexin 26, Amino Acid Substitution, Haplotypes, Sensorineural hearing loss, medicine.symptom, Founder effect
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::268edae124d06e86e333edb583c31744Test
https://doi.org/10.1111/j.1399-0004.2009.01183.xTest -
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المؤلفون: Suat Fitoz, Levent Sennaroglu, S Birnbaum, EB Yüksel Konuk, Mustafa Tekin, Walter E. Nance, Senem Senturk, Ergul Tuncbilek, Filiz Basak Cengiz, Duygu Duman, Armagan Incesulu, H. Ozturkmen Akay, I Cebeci, A Hasanefendioğlu Bayrak, Gülen Eda Utine
المصدر: Clinical Genetics. 73:554-565
مصطلحات موضوعية: Adult, Male, Proband, animal structures, Adolescent, DNA Mutational Analysis, Fibroblast Growth Factor 3, Emissary veins, Deafness, Biology, medicine.disease_cause, Nuclear Family, Genetics, medicine, Microdontia, Humans, Child, Genetics (clinical), Auricle, Mutation, Tooth Abnormalities, Homozygote, Microtia, Infant, Aplasia, Anatomy, medicine.disease, stomatognathic diseases, medicine.anatomical_structure, Ear, Inner, Agenesis, Blood Vessels, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33fe70e30952dd4b415b8449181996c7Test
https://doi.org/10.1111/j.1399-0004.2008.01004.xTest