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Whole-exome sequencing to identify the cause of congenital ..:
Parzefall, Thomas
;
Frohne, Alexandra
;
Koenighofer, Martin
...
European Archives of Oto-Rhino-Laryngology. 274 (2017) 10 - p. 3619-3625 , 2017
Link:
https://doi.org/10.1007/s00405-017-4699-0
RT Journal T1
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation
UL https://suche.suub.uni-bremen.de/peid=cr-10.1007_s00405-017-4699-0&Exemplar=1&LAN=DE A1 Parzefall, Thomas A1 Frohne, Alexandra A1 Koenighofer, Martin A1 Kirchnawy, Andreas A1 Streubel, Berthold A1 Schoefer, Christian A1 Frei, Klemens A1 Lucas, Trevor PB Springer Science and Business Media LLC YR 2017 SN 0937-4477 SN 1434-4726 JF European Archives of Oto-Rhino-Laryngology VO 274 IS 10 SP 3619 OP 3625 LK http://dx.doi.org/https://doi.org/10.1007/s00405-017-4699-0 DO https://doi.org/10.1007/s00405-017-4699-0 SF ELIB - SuUB Bremen
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