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Phenotypic variability of non-syndromic hearing loss in patients heterozygous for both c.35delG of GJB2 and the 342-kb deletion involving GJB6

✍ Scribed by Hanno Bolz; Götz Schade; Stefanie Ehmer; Christian Kothe; Markus Hess; Andreas Gal


Book ID
117534569
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
273 KB
Volume
188
Category
Article
ISSN
0378-5955

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