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European Journal of Human Genetics : EJHG
|
January 16, 2014
Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia
Davut Pehlivan, Ender Karaca, Hatip Aydin, et al.
The Journal of Clinical Investigation
|
January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin
Yavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.
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Showing results (31-40 of 32) with videos related to
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Page
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This site can display upto 32 results.
European Journal of Human Genetics : EJHG
|
January 16, 2014
Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia
Davut Pehlivan, Ender Karaca, Hatip Aydin, et al.
The Journal of Clinical Investigation
|
January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin
Yavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.
Page
of 4