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Publisher : mary ann liebert, inc Subject : deafness Subject : genetic testing
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Academic Journal

A low-cost exon capture method suitable for large-scale screening of genetic deafness by the massively-parallel sequencing approach.

  • Authors : Tang W; Department of Otolaryngology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.; Qian D

Subjects: Gene Targeting*; Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*economics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2012 Jun; Vol. 16 (6), pp. 536-42. Date of Electronic Publication: 2012 Apr 05.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay.

  • Authors : Abe S; Division of Advanced Technology and Development, BML, Inc., Kawagoe-shi, Saitama 350-1101, Japan.; Yamaguchi T

Subjects: DNA Mutational Analysis/DNA Mutational Analysis/DNA Mutational Analysis/*methods ; Deafness/Deafness/Deafness/*diagnosis ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: Genetic testing [Genet Test] 2007 Fall; Vol. 11 (3), pp. 333-40.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 9802546 Publication Model: Print Cited Medium:

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Academic Journal

Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes.

  • Authors : Rydzanicz M; Institute of Human Genetics, Polish Academy of Sciences, Poznań, Poland. ; Wróbel M

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

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2009 Apr; Vol. 13 (2), pp. 167-72.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

A simple method of screening for the common connexin-26 gene 35delG mutation in nonsyndromic neurosensory autosomal recessive deafness.

  • Authors : Fernández-Burriel M; Laboratorio de genética molecular, Servicio de Análisis Clínicos, Hospital Materno-Infantil, 35016-Las Palmas de Gran Canaria, Canary Islands, Spain. ; Rodríguez-Quiñones F

Subjects: Sequence Deletion*; Connexins/Connexins/Connexins/*genetics ; Deafness/Deafness/Deafness/*genetics

  • Source: Genetic testing [Genet Test] 2003 Summer; Vol. 7 (2), pp. 147-9.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 9802546 Publication Model: Print Cited Medium:

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Academic Journal

Stem Cell-Based Therapies for Auditory Hair Cell Regeneration in the Treatment of Hearing Loss.

  • Authors : Cumpata AJ; Doctoral School, 'Grigore T. Popa' University of Medicine and Pharmacy, Iasi, Romania.; Labusca L

Subjects: Hearing Loss*/Hearing Loss*/Hearing Loss*/therapy ; Hearing Loss*/Hearing Loss*/Hearing Loss*/metabolism ; Deafness*/Deafness*/Deafness*/metabolism

  • Source: Tissue engineering. Part B, Reviews [Tissue Eng Part B Rev] 2024 Feb; Vol. 30 (1), pp. 15-28. Date of Electronic Publication: 2023 Aug 10.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101466660 Publication Model: Print-Electronic

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Academic Journal

Audiologic Measures in an Indigenous Community with A2ML1- and FUT2- Related Otitis Media.

  • Authors : Santos-Cortez RLP; Department of Otolaryngology-Head and Neck Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.; Center for Children's Surgery, Children's Hospital Colorado, Aurora, Colorado, USA.

Subjects: Deafness* ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics ; Hearing Loss*/Hearing Loss*/Hearing Loss*/diagnosis

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2023 Jan; Vol. 27 (1), pp. 12-17.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review.

  • Authors : Manyisa N; Division of Human Genetics, Department of Pathology, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.; Adadey SM

Subjects: Deafness*/Deafness*/Deafness*/genetics ; Hearing Loss*/Hearing Loss*/Hearing Loss*/epidemiology ; Hearing Loss*/Hearing Loss*/Hearing Loss*/geneticsNonsyndromic Deafness

  • Source: Omics : a journal of integrative biology [OMICS] 2022 Jan; Vol. 26 (1), pp. 2-18.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101131135 Publication Model: Print Cited

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Academic Journal

Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.

  • Authors : Kannan-Sundhari A; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, USA.; Dr. John T. Macdonald Foundation, Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Oct; Vol. 24 (10), pp. 674-680. Date of Electronic Publication: 2020 Sep Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

A Mutational Analysis of GJB2, SLC26A4, MT-RNA1, and GJB3 in Children with Nonsyndromic Hearing Loss in the Henan Province of China.

  • Authors : Ming L; 1 Key Clinical Laboratory of Henan Province, Department of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University , Zhengzhou, China .; Wang Y

Subjects: Deafness/Deafness/Deafness/*genetics ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics; Adolescent Nonsyndromic Deafness

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2019 Jan; Vol. 23 (1), pp. 51-56. Date of Electronic Publication: 2018 Dec 27.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Clinical Exome Sequencing Identifies a Frameshift Mutation Within the STRC Gene in a United Arab Emirates Family with Profound Nonsyndromic Hearing Loss.

Subjects: Deafness/Deafness/Deafness/*genetics ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics; Adult Nonsyndromic Deafness

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2019 Mar; Vol. 23 (3), pp. 204-208. Date of Electronic Publication: 2019 Feb 13.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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  • 1-10 of  40 results for ""Deafness""