Clinical presentation of DFNB1

Book chapter

Peer reviewed

Wyman T McGuirt, Sai D Prasad, Robert A Cucci, Glenn E Green and Richard J H Smith

Genetic Hearing Impairment: Its Clinical Presentations, pp.113-119

Advances in oto-rhino-laryngology, v. 61, Karger

2002

DOI: 10.1159/000066821

PMID: 12408072

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Mutation

Adolescent

Adult

Audiometry

Child

Child, Preschool

Connexin 26

Connexins - genetics

Genetic Testing

Hearing Loss, Sensorineural - diagnosis

Hearing Loss, Sensorineural - genetics

Humans

Infant

Middle Aged

Polymorphism, Genetic

Title: Subtitle: Clinical presentation of DFNB1
Creators: Wyman T McGuirt - University of Iowa
Sai D Prasad - University of Iowa
Robert A Cucci - University of Iowa
Glenn E Green - University of Iowa
Richard J H Smith - University of Iowa
Resource Type: Book chapter
Publication Details: Genetic Hearing Impairment: Its Clinical Presentations, pp.113-119
Publisher: Karger; New York
Series: Advances in oto-rhino-laryngology; v. 61
DOI: 10.1159/000066821
PMID: 12408072
eISBN: 3318008702; 9783318008708
ISSN: 0065-3071
eISSN: 1662-2847
Grant note: 5-T32-DC0040 / NIDCD NIH HHS R01-DC02842 / NIDCD NIH HHS
Language: English
Date published: 2002
Academic Unit: Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
Record Identifier: 9984256842702771

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