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post·lin·gual (pōst-lingґgwəl) 1. occurring after the development of language. 2. posterior to the tongue or to a lingula.Medical dictionary. 2011.
postlingual fissure — fissura precentralis cerebelli … Medical dictionary
postlingual hearing loss — hearing loss that occurs after the person has learned to speak … Medical dictionary
Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… … Wikipedia
COCH — Coagulation factor C homolog, cochlin (Limulus polyphemus), also known as COCH, is a human gene.cite web | title = Entrez Gene: COCH coagulation factor C homolog, cochlin (Limulus polyphemus)| url =… … Wikipedia
TMPRSS3 — Transmembrane protease, serine 3, also known as TMPRSS3, is a human gene.cite web | title = Entrez Gene: TMPRSS3 transmembrane protease, serine 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=64699|… … Wikipedia
TECTA — Tectorin alpha, also known as TECTA, is a human gene.cite web | title = Entrez Gene: TECTA tectorin alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7007| accessdate = ] PBB Summary section title =… … Wikipedia
EYA4 — Eyes absent homolog 4 (Drosophila), also known as EYA4, is a human gene.cite web | title = Entrez Gene: EYA4 eyes absent homolog 4 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2070|… … Wikipedia
TMC1 — Transmembrane channel like 1, also known as TMC1, is a human gene.cite web | title = Entrez Gene: TMC1 transmembrane channel like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=117531| accessdate = ] PBB … Wikipedia
Usher-Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie H90.3 … Deutsch Wikipedia
Usher Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie … Deutsch Wikipedia
