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1مورد إلكتروني
مصطلحات الفهرس: human, cochlea, GJB2, GJB6, RNAscope, in situ hybridization, Biochemistry and Molecular Biology, Biokemi och molekylärbiologi, Article in journal, info:eu-repo/semantics/article, text
URL:
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-486974Test
Frontiers in Molecular Neuroscience, 1662-5099, 2022, 15 -
2مورد إلكتروني
مصطلحات الفهرس: human, cochlea, GJB2, GJB6, RNAscope, in situ hybridization, Biochemistry and Molecular Biology, Biokemi och molekylärbiologi, Article in journal, info:eu-repo/semantics/article, text
URL:
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-486974Test
Frontiers in Molecular Neuroscience, 1662-5099, 2022, 15 -
3مورد إلكتروني
مصطلحات الفهرس: human, cochlea, GJB2, GJB6, RNAscope, in situ hybridization, Biochemistry and Molecular Biology, Biokemi och molekylärbiologi, Article in journal, info:eu-repo/semantics/article, text
URL:
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-486974Test
Frontiers in Molecular Neuroscience, 1662-5099, 2022, 15 -
4مورد إلكتروني
مصطلحات الفهرس: human, cochlea, GJB2, GJB6, RNAscope, in situ hybridization, Biochemistry and Molecular Biology, Biokemi och molekylärbiologi, Article in journal, info:eu-repo/semantics/article, text
URL:
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-486974Test
Frontiers in Molecular Neuroscience, 1662-5099, 2022, 15 -
5مورد إلكتروني
مصطلحات الفهرس: human, cochlea, GJB2, GJB6, RNAscope, in situ hybridization, Biochemistry and Molecular Biology, Biokemi och molekylärbiologi, Article in journal, info:eu-repo/semantics/article, text
URL:
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-486974Test
Frontiers in Molecular Neuroscience, 1662-5099, 2022, 15 -
6مورد إلكتروني
المصدر: Research outputs 2013
مصطلحات الفهرس: C.35delG, Connexin, Consanguinity, GJB2, Nonsyndromic hearing impairment, P.Arg75 Gln connexin 26, connexin 30, adolescent, adult, article, Brazil, child, ethnicity, familial disease, female, gene, gene mutation, genetic heterogeneity, GJB2 gene, GJB6 gene, hearing impairment, heterozygote, homozygote, human, major clinical study, male, MTRNR1 gene, nonsyndromic hearing impairment, preschool child, priority journal, school child, Adolescent, Adult, Aged, Child, Preschool, Connexins, Ethnic Groups, Female, Hearing Loss, Humans, Male, Middle Aged, Mutation, Orphan Nuclear Receptors, Polymerase Chain Reaction, Polymorphism, Restriction Fragment Length, Rural Population, Young Adult, Medical Genetics, Speech and Hearing Science, text