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Targeted and genomewide NGS data disqualify mutations in MYO1A, the "DFNA48 gene", as a cause of deafness. [electronic resource] by
- Eisenberger, Tobias
- Di Donato, Nataliya
- Baig, Shahid M
- Neuhaus, Christine
- Beyer, Anke
- Decker, Eva
- Mürbe, Dirk
- Decker, Christian
- Bergmann, Carsten
- Bolz, Hanno J
Producer: 20141212
In:
Human mutation vol. 35
Availability: No items available.
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A C-terminal nonsense mutation links PTPRQ with autosomal-dominant hearing loss, DFNA73. [electronic resource] by
- Eisenberger, Tobias
- Di Donato, Nataliya
- Decker, Christian
- Delle Vedove, Andrea
- Neuhaus, Christine
- Nürnberg, Gudrun
- Toliat, Mohammad
- Nürnberg, Peter
- Mürbe, Dirk
- Bolz, Hanno Jörn
Producer: 20181017
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 20
Availability: No items available.
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