-
[文献書誌] Abe S: "Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification"J Hum Genet. 48・3. 142-149 (2003)
-
[文献書誌] Park HJ: "Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians : global implications for the epidemiology of deafness"J Med Genet. 40・4. 242-248 (2003)
-
[文献書誌] Usami S: "Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease"Eur J Hum Genet. 11・10. 744-748 (2003)
-
[文献書誌] Abe S: "Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss"J Hum Genet. 48・11. 564-570 (2003)
-
[文献書誌] Tsukamoto K: "Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct : a unique spectrum of mutations in Japanese"Eur J Hum Gene. 11・12. 916-922 (2003)
-
[文献書誌] 宇佐美 真一: "遺伝カウンセリングマニュアル(福嶋義光編) : 耳鼻科疾患"本郷 允彦. 1,360 (2003)
