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The EuroBiotech Journal
Volume 4 (2020): Issue 4 (October 2020)
Open Access
The Biennial report: The collaboration between MAGI Research, Diagnosis and Treatment Center of Genetic and Rare Diseases and Near East University DESAM Institute
Mahmut Cerkez Ergoren
Mahmut Cerkez Ergoren
,
Elena Manara
Elena Manara
,
Stefano Paolacci
Stefano Paolacci
,
Havva Cobanogullari
Havva Cobanogullari
,
Gulten Tuncel
Gulten Tuncel
,
Meryem Betmezoglu
Meryem Betmezoglu
,
Matteo Bertelli
Matteo Bertelli
and
Tamer Sanlidag
Tamer Sanlidag
| Oct 21, 2020
The EuroBiotech Journal
Volume 4 (2020): Issue 4 (October 2020)
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Article Category:
Brief Reports
Published Online:
Oct 21, 2020
Page range:
167 - 170
DOI:
https://doi.org/10.2478/ebtj-2020-0020
Keywords
rare-disease
,
genomics
,
high-throughput DNA sequencing
,
variants
,
genetic disorders
© 2020 Mahmut Cerkez Ergoren, Elena Manara, Stefano Paolacci, Havva Cobanogullari, Gulten Tuncel, Meryem Betmezoglu, Matteo Bertelli, Tamer Sanlidag, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Some studied diseases and their scientific/diagnostic significance to the literature