Copy number variants are a common cause of non-syndromic hearing loss

Overview of attention for article published in Genome Medicine, May 2014

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dimensions_citation: 148 Dimensions

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mendeley: 106 Mendeley
citeulike: 3 CiteULike

Summary X Dimensions citations

So far, Dimensions has found 148 publications that cite this research output.

148

The most recent citing publications are shown below. View all 148 publications that cite this research output on Dimensions.

Identification of novel gene variants causing autosomal recessive non-syndromic hearing loss in Iranian families

Preprint in Research Square (February 2024)

The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar

Article in Scientific Reports (February 2024)

Function and Evolution of Repeated DNA Sequences

Monograph (December 2023)

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