A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

類似資料

• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.
  著者:: Brown, M R, 等
  出版事項: (1997)
• A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus
  著者:: Van Camp, G., 等
  出版事項: (1999)
• A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.
  著者:: Fukushima, K, 等
  出版事項: (1999)
• Nonsyndromic hearing impairment: unparalleled heterogeneity.
  著者:: Van Camp, G, 等
  出版事項: (1997)
• Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss
  著者:: Bahmad, Fayez, 等
  出版事項: (2008)