Tuba DİNÇER, Samiye Çilem BİLGİNER, Bayram TORAMAN, Gülden YORGANCIOĞLU BUDAK, Hülya KAYSERİLİ, Ersan KALAY

Two male patients from an extended seven generation Turkish family diagnosed with Renpenning syndrome: identifying the causative mutation and review of the literature

The European Research Journal

2022-Cilt: 8 - Sayı: 3

420-427

Renpenning syndrome, PQBP1, intellectual disability, microcephaly

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