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1. A case of U2AF2 -related developmental disorder: long-term follow-up and expansion of the phenotype.

MULAYIM M. F., DEMİRBAŞ M. H., Percin F. E., ARHAN E., KAYHAN G.
Clinical dysmorphology , vol.33, no.4, pp.171-175, 2024 (SCI-Expanded) identifier identifier identifier
Papers Presented at Peer-Reviewed Scientific Conferences 1

1. Genetic Insights into Retinoblastoma: Somatic Mosaicism and Clinical Correlations

Mulayım M. F., Vural Ö., Atalay H. T., Kayhan G.
International Hereditary Cancers Congress, Antalya, Turkey, 6 - 08 February 2025, vol.36, pp.32, (Summary Text) Creative Commons License
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UN Sustainable Development Goals