Articles with public access mandates - COŞKUN SILANLearn more
Available somewhere: 2
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN
K Lehmann, P Seemann, F Silan, TO Goecke, S Irgang, KW Kjaer, ...
The American Journal of Human Genetics 81 (2), 388-396, 2007
Mandates: German Research Foundation
Blau syndrome with a rare mutation in exon 9 of NOD2 gene
J Velickovic, F Silan, FD Bir, C Silan, B Albuz, O Ozdemir
Autoimmunity 52 (7-8), 256-263, 2019
Mandates: Ministry of Education, Science and Technological Development of the Republic …
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