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Academic Journal

The responsible genes in Japanese deafness patients and clinical application using Invader assay.

Subjects: GENETICS of deafness; DEAFNESS; DEAF people

  • Source: Acta Oto-Laryngologica. Apr2008, Vol. 128 Issue 4, p446-454. 9p. 3 Diagrams, 1 Chart.

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Academic Journal

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

Subjects: DEAFNESS; GENES; HUMAN chromosome abnormality diagnosisCHINA

  • Source: Acta Oto-Laryngologica. Mar2008, Vol. 128 Issue 3, p297-303. 7p. 3 Charts, 2 Graphs.

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Academic Journal

Deafness gene mutations in newborns in Beijing.

Subjects: GENETICS of deafness; ALLELES; CARRIER state (Communicable diseases)CHINA

  • Source: Acta Oto-Laryngologica. May2016, Vol. 136 Issue 5, p475-479. 5p.

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Academic Journal

A nationwide epidemiologic, clinical, genetic study of Usher syndrome in Japan.

Subjects: HOSPITALS; SOCIAL support; DEAFNESSJAPAN

  • Source: Acta Oto-Laryngologica. Sep 2021, Vol. 141 Issue 9, p841-846. 6p.

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