Hearing impairment in a female infant with interstitial deletion of 2q24.1q24.3-Reference-Cited by-同舟云学术

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Hearing impairment in a female infant with interstitial deletion of 2q24.1q24.3

Published:2017-03-30 Issue:4 Volume:57 Page:118-121
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenital Anomalies

Author:

Ono Hiroaki¹,Kurosawa Kenji²,Wakamatsu Nobuaki³,Masuda Shin⁴

Affiliation:

1. The Department of Pediatrics; Hiroshima Prefectural Hospital; Hiroshima Japan

2. Division of Medical Genetics; Kanagawa Children's Medical Center; Yokohama Kanagawa Japan

3. Department of Genetics, Institute for Developmental Research; Aichi Human Service Center; Kasugai Aichi Japan

4. The Department of Pediatric rehabilitation; Hiroshima Prefectural Hospital; Hiroshima Japan

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cga.12207/fullpdf

Reference4 articles.

1. A de novo 2.3 Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl;Belengeanu;Gene,2014

2. High prevalence of inner-ear and/or internal auditory canal malformations in children with unilateral sensorineural hearing loss;Masuda;Int J Pediatr Otorhinolaryngol,2013

3. Putting into practice domain-linear motif interaction predictions for exploration of protein networks;Luck;PLoS One,2011

4. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C;Verpy;Nat Genet,2000

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness;Cytogenetic and Genome Research;2022

2. Tumor predisposition in an individual with chromosomal rearrangements of 1q31.2‐q41 encompassing cell division cycle protein 73;Congenital Anomalies;2019-10-21

3. Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing RPL5;Human Genome Variation;2019-08-08

4. Developmental delay and dysmorphic features in a girl with a de novo 5.4 Mb deletion of 13q12.11‐q12.13;Congenital Anomalies;2019-06-27

5. 2q24 deletion in a 9-month old girl with anal atresia, hearing impairment, and hypotonia;International Journal of Pediatric Otorhinolaryngology;2018-06

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