Cordula Neuner
Wuerzburg, BY, Germany
Last Updated: 09/26/2026
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Found 8 publications
FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.
Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2026
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.
Journal: BMC medical genetics
Published: March 12, 2014
Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 24, 2014
DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics.
Journal: Clinical genetics
Published: October 15, 2013
A Boy with an LCR3/4-Flanked 10q22.3q23.2 Microdeletion and Uncommon Phenotypic Features.
Journal: Molecular syndromology
Published: August 07, 2013
Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.
Journal: Molecular syndromology
Published: August 05, 2013
Confirmation of GRHL2 as the gene for the DFNA28 locus.
Journal: American journal of medical genetics. Part A
Published: February 14, 2013
Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6.
Journal: European journal of human genetics : EJHG
Published: October 30, 2012
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Last Updated: 09/26/2026