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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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Education Full Text (H.W. Wilson)

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Whole-exome sequencing for screening noise-induced hearing loss susceptibility genes.

• Authors : Fan, Boya (AUTHOR); Wang, Gang (AUTHOR); Liu, Gang (AUTHOR)

Subjects: SEQUENCE analysis; STAINS & staining (Microscopy); COCHLEA

• Source: Acta Oto-Laryngologica. May2023, Vol. 143 Issue 5, p408-415. 8p.

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

• Authors : Yoshimura, Hidekane (AUTHOR); Nishio, Shin-ya (AUTHOR); Isaka, Yuichi (AUTHOR)

Subjects: HOSPITALS; SOCIAL support; DEAFNESSJAPAN

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

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Explaining Alport syndrome—lessons from the adult nephrology clinic.

• Authors : Mabillard, Holly; Ryan, Rebecca; Tzoumas, Nik

Subjects: ALPORT syndrome; KIDNEY diseases; KIDNEY failure

• Source: Journal of Rare Diseases; 5/13/2024, Vol. 3 Issue 1, p1-26, 26p

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Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China.

• Authors : Zhang, Meng (AUTHOR); Han, Yuechen (AUTHOR); Zhang, Fengguo (AUTHOR)

Subjects: GENETICS of deafness; GENES; GENETIC disordersCHINA

• Source: Acta Oto-Laryngologica. Jul2019, Vol. 139 Issue 7, p612-617. 6p.

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The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10‐year follow‐up observation study and literature review.

• Authors : Zheng, Shasha; Wang, Juanjuan; Sun, Minxian

Subjects: LITERATURE reviews; DEAFNESS; MITOCHONDRIAL DNA

• Source: Clinical Case Reports; Feb2024, Vol. 12 Issue 2, p1-9, 9p

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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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