Researcher: Kaya, Mert
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Kaya, Mert
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Publication Metadata only Oculo-auricular syndrome in a new multiplex family does not link to HMX1 or its downstream enhancer(Springernature, 2024) Bertoli-Avella, Aida; Altunoğlu, Umut; Kaya, Mert; Satkın, Nihan Bilge; Börklü Yücel, Esra; Graduate School of Health Sciences; School of Medicine; Koç University HospitalPublication Metadata only Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies(Springernature, 2023) Kalayci, Tugba; Uyguner, Zehra Oya; Altunoğlu, Umut; Kaya, Mert; School of Medicine; Graduate School of Health Sciences