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Personal utility of genomic sequencing for infants with congenital deafness.

• Authors : Tutty E; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.

Subjects: Genetic Testing* ; Genomics*; Deafness/Deafness/Deafness/*diagnosis

• Source: American journal of medical genetics. Part A [Am J Med Genet A] 2021 Dec; Vol. 185 (12), pp. 3634-3643. Date of Electronic Publication: 2021 Jun 29.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Advancing genetic testing for deafness with genomic technology.

• Authors : Shearer AE; Department of Otolaryngology-Head and Neck Surgery, Molecular Otolaryngology & Renal Research Labs, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.; Black-Ziegelbein EA

Subjects: Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Genomics/Genomics/Genomics/*methods

• Source: Journal of medical genetics [J Med Genet] 2013 Sep; Vol. 50 (9), pp. 627-34. Date of Electronic Publication: 2013 Jun 26.Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet

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Hereditary deafness carrier screening in 9,993 Chinese individuals.

• Authors : Yanqiu Liu; Lei Wang; Lanlai Yuan

Subjects: MEDICAL screening; DEAFNESS; GENETIC testingCHINA

• Source: Frontiers in Genetics; 2024, p1-7, 7p

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Genetic screening of common genetic deafness in 60,391 women of childbearing age and intervention of birth defects.

• Authors : Linyuan Niu; Liqin Liu; Jinjun Tian

Subjects: GENETIC testing; CHILDBEARING age; DEAFNESS

• Source: Archives of Medical Science; Jan2024, Vol. 20 Issue 1, p113-123, 11p

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Education Full Text (H.W. Wilson)

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Retrospective Analysis of the Outcomes of Genetic Testing in Patients Suspected to Have Hereditary Hearing Loss or Deafness.

• Authors : Bowden, Acacia; Hubbel, Alexandra; Smith, Lindsay

Subjects: GENETICS of deafness; COCHLEAR implants; SEQUENCE analysis

• Source: American Journal of Audiology. Mar2024, Vol. 33 Issue 1, p233-241. 9p.

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

• Authors : Usami, Shin-Ichi (AUTHOR); Wagatsuma, Michio (AUTHOR); Fukuoka, Hisakuni (AUTHOR)

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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Advances in hereditary deafness.

• Authors : Tekin, Mustafa; Arnos, Kathleen S; Pandya, Arti

Subjects: GENETICS of deafness; DEAFNESS; MEDICAL screening

• Source: Lancet. 9/29/2001, Vol. 358 Issue 9287, p1082. 9p. 1 Diagram, 2 Charts.

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

• Authors : Guo, Yu-Fen (AUTHOR); Liu, Xiao-Wen (AUTHOR); Guan, Jing (AUTHOR)

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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Case report: Prenatal diagnosis in the fetus of a couple with both thalassemia and deafness genes.

• Authors : Youqiong Li; Liang Liang; Jinping Bai

Subjects: PRENATAL diagnosis; DEAFNESS; FETUS

• Source: Frontiers in Genetics; 2023, p1-5, 5p

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