Sensorineural deafness, hydrocephalus and structural brain abnormalities in two sisters: The Chudley–McCullough syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference17 articles.
1. The genetics of hearing loss
2. Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: A newly described autosomal recessive disorder
3. Mitochondrial Deafness
4. , . 1995. Hereditary hearing loss and its syndromes. Oxford monographs on medical genetics N.28. New York: Oxford University Press.
5. Bilateral sensorineural deafness, partial agenesis of the corpus callosum, and arachnoid cysts in two sisters
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1. The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact;Fluids and Barriers of the CNS;2024-03-04
2. Chudley-McCullough syndrome;Radiopaedia.org;2022-06-24
3. Cochlear implant in a subject affected by the Chudley-McCullough Syndrome;Cochlear Implants International;2019-03-25
4. Chudley–McCullough Syndrome;Journal of Clinical Imaging Science;2018-11-15
5. Prenatal diagnosis of Chudley-McCullough syndrome;American Journal of Medical Genetics Part A;2016-06-17
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