Chan-Ho. Hwang, et.al., Noggin heterozygous mice: an animal model for congenital conductive hearing loss in humans., Human molecular genetics, 2008, 17

http://rdf.ncbi.nlm.nih.gov/pubmed/18096605

Chan-Ho. Hwang, et.al., Noggin heterozygous mice: an animal model for congenital conductive hearing loss in humans., Human molecular genetics, 2008, 17

pubmed

表現型アノテーション

http://purl.org/net/cito/citesAsAuthority

• abnormal malleus morphology_Nog<tm1Amc>/Nog<tm1Amc>
  http://metadb.riken.jp/0000029B6129S1Nogtm1AmcNogtm1AmcNogtm1AmcNogtm1Amc
• abnormal middle ear morphology_Nog<tm1Amc>/Nog<+>
  http://metadb.riken.jp/0000049D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog
• fusion of middle ear ossicles_Nog<tm1Amc>/Nog<tm1Amc>
  http://metadb.riken.jp/0003740B6129S1Nogtm1AmcNogtm1AmcNogtm1AmcNogtm1Amc
• conductive hearing loss_Nog<tm1Amc>/Nog<+>
  http://metadb.riken.jp/0004739D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog
• abnormal middle ear ossicle morphology_Nog<tm1Amc>/Nog<+>
  http://metadb.riken.jp/0005105D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog
• abnormal incus morphology_Nog<tm1Amc>/Nog<tm1Amc>
  http://metadb.riken.jp/0005106B6129S1Nogtm1AmcNogtm1AmcNogtm1AmcNogtm1Amc
他4件を見る
• abnormal stapes morphology_Nog<tm1Amc>/Nog<+>
  http://metadb.riken.jp/0005107D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog
• impaired hearing_Nog<tm1Amc>/Nog<+>
  http://metadb.riken.jp/0006325D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog
• abnormal styloid process morphology_Nog<tm1Amc>/Nog<+>
  http://metadb.riken.jp/0008023D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog
• increased or absent threshold for auditory brainstem response_Nog<tm1Amc>/Nog<+>
  http://metadb.riken.jp/0011967D1129S1Nogtm1AmcNogtm1AmcNogNogtm1AmcNog