Dr. Öğr. Üyesi GÜLSÜM KAYHAN

Ödüller

• Kasım 2022 PREDICTION OF GENOTYPE POSITIVITY IN PATIENTS WITH KIDNEY DISEASE USING MACHINE LEARNING

  Bantao

• Mart 2019 A combined oxidative phosphoriylation deficiency 10 case in a neon-consanguineous family

  Erciyes Genetik Günleri 2019 Kayseri

• Mart 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

• Mart 2017 Without the hotspot mutation, Trismus-pseudocamptodactyly syndrome is possible?

  Erciyes Genetik Günleri Kayseri