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Auditory Detection Thresholds and Cochlear Resistivity Differ Between Pediatric Cochlear Implant Listeners With Enlarged Vestibular Aqueduct and Those With Connexin-26 Mutations.

• Authors : Jahn, Kelly N.^1,2, ; Bergan, Molly D.³; Arenberg, Julie G.^1,2

• Source: American Journal of Audiology; Mar2020, Vol. 29 Issue 1, p23-34, 12p, 3 Charts, 4 Graphs

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Deafness Gene Mutations in Newborns in the Foshan Area of South China With Bloodspot-Based Genetic Screening Tests.

• Authors : Cao S; Department of Laboratory Medicine, The Second Clinical College of Guangzhou University of Chinese Medicine, Guangdong, China.; Sha Y

Subjects: Connexin 26/Connexin 26/Connexin 26/*genetics ; Connexins/Connexins/Connexins/*genetics ; Deafness/Deafness/Deafness/*genetics

• Source: American journal of audiology [Am J Audiol] 2020 Jun 08; Vol. 29 (2), pp. 165-169. Date of Electronic Publication: 2020 Mar 24.Publisher: American Speech-Language-Hearing Association Country of Publication: United States NLM ID: 9114917 Publication Model:

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Newborn Screening of Genetic Mutations in Common Deafness Genes With Bloodspot-Based Gene Chip Array.

• Authors : He X; Clinical Laboratory Center, General Hospital of Ningxia Medical University, Yinchuan, China.; Ningxia Key Laboratory of Clinical and Pathogenic Microbiology, General Hospital of Ningxia Medical University, Yinchuan, China.

Subjects: DNA Mutational Analysis*; Connexins/Connexins/Connexins/*genetics ; Deafness/Deafness/Deafness/*genetics

• Source: American journal of audiology [Am J Audiol] 2018 Mar 08; Vol. 27 (1), pp. 57-66.Publisher: American Speech-Language-Hearing Association Country of Publication: United States NLM ID: 9114917 Publication Model:

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Guidelines for Audiologists on the Benefits and Limitations of Genetic Testing.

• Authors : Mercer D

Subjects: Audiology* ; Genetic Testing* ; Practice Guidelines as Topic*

• Source: American journal of audiology [Am J Audiol] 2015 Dec; Vol. 24 (4), pp. 451-61.Publisher: American Speech-Language-Hearing Association Country of Publication: United States NLM ID: 9114917 Publication Model:

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X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4.

• Authors : Anger GJ; Crocker S; McKenzie K

Subjects: Chromosome Inversion*; Chromosomes, Human, X/Chromosomes, Human, X/Chromosomes, Human, X/*genetics ; Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/*genetics Progressive hearing loss stapes fixation

• Source: American journal of audiology [Am J Audiol] 2014 Mar; Vol. 23 (1), pp. 1-6.Publisher: American Speech-Language-Hearing Association Country of Publication: United States NLM ID: 9114917 Publication Model:

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