Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome-Reference-Cited by-同舟云学术

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Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome

Published:2016-09-08 Issue:11 Volume:170 Page:2975-2983
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Loos Elke¹,Verhaert Nicolas¹²,Willaert Annelore¹,Devriendt Koenraad³,Swillen Ann³,Hermans Robert⁴,Op de Beeck Katya⁴,Hens Greet¹²

Affiliation:

1. Department of Otorhinolaryngology-Head and Neck Surgery; University Hospitals Leuven; Leuven Belgium

2. Department of Neurosciences, ExpORL, KU Leuven; University of Leuven; Leuven Belgium

3. Centre for Human Genetics; University Hospitals Leuven; Leuven Belgium

4. Department of Radiology; University Hospitals Leuven; Leuven Belgium

Funder

Fonds Wetenschappelijk Onderzoek

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference54 articles.

1. Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients;Arnold;Hum Mol Genet,2006

2. The international 22q11.2 deletion syndrome consortium. practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;J Pediatr,2011

3. Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome;Bish;Neurosci Lett,2006

4. Cooperative function of Tbx1 and Brn4 in the periotic mesenchyme is necessary for cochlea formation;Braunstein;J Assoc Res Otolaryngol,2008

5. Estimated Risks of Radiation-induced fatal cancer from pediatric CT;Brenner;Am J Roentgenol,2001

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1. Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2;American Journal of Medical Genetics Part A;2023-11-02

2. Conductive Hearing Loss in Children;Neuroimaging Clinics of North America;2023-11

3. Syndromic Hearing Loss in Children;Neuroimaging Clinics of North America;2023-11

4. Otorhinologic Disorders in 22q11.2 Deletion Syndrome;Otolaryngology–Head and Neck Surgery;2023-03-23

5. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03

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