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Subject : genetic testing Subject : genetics Geographic : taiwan
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Academic Journal

Prospective Mutation Screening of Three Common Deafness Genes in a Large Taiwanese Cohort with Idiopathic Bilateral Sensorineural Hearing Impairment Reveals a Difference in the Results between Families from Hospitals and Those from Rehabilitation Facilities

Subjects: GENETICS of deafness; HUMAN chromosome abnormality diagnosis; GENETIC mutationTAIWAN

  • Source: Audiology & Neurotology; 2008, Vol. 13 Issue 3, p172-181, 10p, 7 Charts

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Academic Journal

Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan.

  • Authors : Lu CY; Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.; Tsao PN

Subjects: Audiometry*; Cytomegalovirus Infections/Cytomegalovirus Infections/Cytomegalovirus Infections/*diagnosis ; Deafness/Deafness/Deafness/*diagnosis

  • Source: The Journal of pediatrics [J Pediatr] 2018 Aug; Vol. 199, pp. 144-150.e1. Date of Electronic Publication: 2018 Apr 19.Publisher: Mosby Country of Publication: United States NLM ID: 0375410 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-6833

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Academic Journal

Impact of Low Birth Weight Child on Maternal Labour Force Participation: Evidence from Taiwan.

Subjects: LOW birth weight; FETAL growth retardation; RISK factors in premature laborTAIWAN

  • Source: Pacific Economic Review; Oct2014, Vol. 19 Issue 4, p483-501, 19p

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Academic Journal

Phenotypic Analyses and Mutation Screening of the SLC26A4 and FOXI1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (DFNB4) or Pendred Syndrome.

Subjects: GENETIC polymorphisms; VESTIBULAR apparatus diseases; GENETICSTAIWAN

  • Source: Audiology & Neurotology; 2010, Vol. 15 Issue 1, p57-66, 10p, 6 Charts, 1 Graph

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Academic Journal

Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan.

Subjects: *DEAFNESS in children; *MEDICAL screening; *GENETICS of disease susceptibilityTAIWAN

  • Source: International Journal of Pediatric Otorhinolaryngology. Apr2015, Vol. 79 Issue 4, p584-590. 7p.

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Academic Journal

Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment.

  • Authors : Wu CC; Department of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.; Lu YC

Subjects: Mutation*; DNA Mutational Analysis/DNA Mutational Analysis/DNA Mutational Analysis/*methods ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: The Laryngoscope [Laryngoscope] 2009 Dec; Vol. 119 (12), pp. 2411-6.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 8607378 Publication Model: Print Cited Medium: Internet ISSN: 1531-4995

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  • 1-6 of  6 results for ""Deafness""