Limitations of hearing screening in newborns with PDS mutations

International Journal of Pediatric Otorhinolaryngology

Volumn 77, Issue 5, 2013, Pages 833-837

  Kim, Bo Gyung ^a   Shin, Joong Wook ^a,b   Park, Hong Joon ^b   Kim, Jung Min ^a   Kim, Un Kyung ^c   Choi, Jae Young ^a  

^a Yonsei University College of Medicine   (South Korea)

^b Soree Ear Clinic   (South Korea)

^c Kyungpook National University   (South Korea)

Author keywords

Habilitation; PDS; Pendrin; Universal newborn hearing screening

Indexed keywords

PENDRIN;

ARTICLE; AUDITORY SCREENING; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DIAGNOSTIC VALUE; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC SCREENING; HUMAN; INFANT; INTERVIEW; MALE; MEDICAL HISTORY; MUTATION RATE; NEWBORN SCREENING; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; VESTIBULE AQUEDUCT;

CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC TESTING; HEARING LOSS, SENSORINEURAL; HEARING TESTS; HUMANS; INFANT; INFANT, NEWBORN; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION; NEONATAL SCREENING; PREVALENCE; RETROSPECTIVE STUDIES;

EID: 84876731523     PISSN: 01655876     EISSN: 18728464     Source Type: Journal    
DOI: 10.1016/j.ijporl.2013.02.023     Document Type: Article

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