A genetic approach to the child with sensorineural hearing loss

Seminars in Perinatology

Volumn 29, Issue 3 SPEC. ISS., 2005, Pages 173-181

  Rehm, Heidi L ^a,b,c,d  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b PARTNERS HEALTHCARE   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

^d NONE   (United States)

Author keywords

Deafness; Genetic; Genetic tests; Hearing loss

Indexed keywords

AMIKACIN; AMINOGLYCOSIDE; ANTIBIOTIC AGENT; CONNEXIN 26; CONNEXIN 30; DIURETIC AGENT; FUROSEMIDE; GENTAMICIN; INFLUENZA VACCINE; RIBOSOME RNA; RUBELLA VACCINE; TOBRAMYCIN; TRANSCRIPTION FACTOR PAX3; TRANSCRIPTION FACTOR SOX10;

ALPORT SYNDROME; AUDIOLOGY; BACTERIAL MENINGITIS; BRANCHIOOTORENAL SYNDROME; CLINICAL FEATURE; COCHLEA PROSTHESIS; COMPUTER ASSISTED TOMOGRAPHY; CYTOMEGALOVIRUS INFECTION; DIFFERENTIAL DIAGNOSIS; ETHICS; FAMILY HISTORY; GENE; GENE MUTATION; GENETIC COUNSELING; GENETICS; HEARING AID; HUMAN; HYPERBILIRUBINEMIA; LONG QT SYNDROME; MOLECULAR GENETICS; NEUROFIBROMATOSIS; NEUROTOXICITY; NEWBORN SCREENING; NUCLEAR MAGNETIC RESONANCE IMAGING; OTITIS MEDIA; OTOFERLIN GENE; PENDRED SYNDROME; PERCEPTION DEAFNESS; PRIORITY JOURNAL; REVIEW; RHESUS INCOMPATIBILITY; RISK FACTOR; RUBELLA; STICKLER SYNDROME; USHER SYNDROME; VACCINATION; WAARDENBURG SYNDROME;

EID: 21344472122     PISSN: 01460005     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.semperi.2004.12.002     Document Type: Review

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