eP263: A pathogenic deletion at 13q32.1q33.1 presenting with bilateral sensorineural hearing loss and pigmentation anomalies, mimicking Waardenburg syndrome

Abstract

Open access

Peer reviewed

Moon Ley Tung, Taylor Warner, Hannah Bombei, Nicole Safina and Jaime Nagy

Genetics in medicine, Vol.24(3), pp.S166-S167

03/2022

DOI: 10.1016/j.gim.2022.01.298

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Published (Version of record) Open Access

Title: Subtitle: eP263: A pathogenic deletion at 13q32.1q33.1 presenting with bilateral sensorineural hearing loss and pigmentation anomalies, mimicking Waardenburg syndrome
Creators: Moon Ley Tung - University of Iowa
Taylor Warner - University of Iowa
Hannah Bombei - University of Iowa
Nicole Safina - University of Iowa
Jaime Nagy - Stead Family Department of Pediatrics, Division of Medical Genetics and Genomics, University of Iowa
Resource Type: Abstract
Publication Details: Genetics in medicine, Vol.24(3), pp.S166-S167
DOI: 10.1016/j.gim.2022.01.298
ISSN: 1098-3600
eISSN: 1530-0366
Publisher: Elsevier Inc
Language: English
Date published: 03/2022
Academic Unit: Stead Family Department of Pediatrics; Medical Genetics and Genomics
Record Identifier: 9984354382302771

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