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Clinical Otolaryngology
Volumn 32, Issue 3, 2007, Pages 226-227
Addressing the challenges of genetic screening for deafness [22]
Author keywords

[No Author keywords available]
Indexed keywords

AUTOSOMAL RECESSIVE INHERITANCE; CONSANGUINEOUS MARRIAGE; CONSANGUINITY; ETHNIC GROUP; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC SCREENING; GENOTYPE; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; LETTER; MICROSATELLITE MARKER; MOLECULAR GENETICS; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SCREENING TEST; SEQUENCE ANALYSIS;
EID: 34249911465     PISSN: 17494478     EISSN: 17494486     Source Type: Journal    
DOI: 10.1111/j.1365-2273.2007.01430.x     Document Type: Letter
Times cited : (1)
References (6)
  • 1
    • 34249912093 scopus 로고    scopus 로고
    • Hereditary Hearing Loss Homepage. Available at: (accessed 20 April 2007)
    • Hereditary Hearing Loss Homepage. Available at: http://webh01.ua.ac.be/ hhh (accessed 20 April 2007)
  • 2
    • 12744269573 scopus 로고    scopus 로고
    • Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment
    • Santos R.L., Wajid M. Pham T.L. (2005) Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment. Clin. Genet. 67, 61 68
    • (2005) Clin. Genet. , vol.67 , pp. 61-68
    • Santos, R.L.1    Wajid, M.2    Pham, T.L.3
  • 3
    • 33745723710 scopus 로고    scopus 로고
    • Mutations of human TMHS cause recessively inherited non-syndromic hearing loss
    • Shabbir M.I., Ahmed Z.M., Khan S.Y. et al. (2006) Mutations of human TMHS cause recessively inherited non-syndromic hearing loss. J. Med. Genet. 43, 634 640
    • (2006) J. Med. Genet. , vol.43 , pp. 634-640
    • Shabbir, M.I.1    Ahmed, Z.M.2    Khan, S.Y.3
  • 4
    • 33746845210 scopus 로고    scopus 로고
    • Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: A new approach for newborn screening follow-up
    • Gardner P., Oitmaa E., Messner A. et al. (2006) Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: a new approach for newborn screening follow-up. Paediatrics 118, 985 994
    • (2006) Paediatrics , vol.118 , pp. 985-994
    • Gardner, P.1    Oitmaa, E.2    Messner, A.3
  • 5
    • 33748612427 scopus 로고    scopus 로고
    • Detection of mutations in genes associated with hearing loss using a microarray-based approach
    • Siemering K., Manji S.S., Hutchison W.M. et al. (2006) Detection of mutations in genes associated with hearing loss using a microarray-based approach. J. Mol. Diagn. 8, 483 489
    • (2006) J. Mol. Diagn. , vol.8 , pp. 483-489
    • Siemering, K.1    Manji, S.S.2    Hutchison, W.M.3
  • 6
    • 33847282820 scopus 로고    scopus 로고
    • Development of a genotyping microarray for usher syndrome
    • Cremers F.P., Kimberling W.J., Kulm M. et al. (2006) Development of a genotyping microarray for usher syndrome. J. Med. Genet. 44, 153 160.
    • (2006) J. Med. Genet. , vol.44 , pp. 153-160
    • Cremers, F.P.1    Kimberling, W.J.2    Kulm, M.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.