Publication
261
Open Access
21
Awards
4
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November 2022 PREDICTION OF GENOTYPE POSITIVITY IN PATIENTS WITH KIDNEY DISEASE USING MACHINE LEARNING
Bantao
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March 2019 A combined oxidative phosphoriylation deficiency 10 case in a neon-consanguineous family
Erciyes Genetik Günleri 2019 Kayseri
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March 2018 A patient with two syndrome due to paternal uniparental disomy of chromosome 2 (pUPD2) related with homozygous novel mutations of the RAB3GAP1 and UNC80 genes
Erciyes Genetik Günleri 2018 Kayseri
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March 2017 Without the hotspot mutation, Trismus-pseudocamptodactyly syndrome is possible?
Erciyes Genetik Günleri Kayseri