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Genetic and Phenotypic Analysis of Patients with Mucopolysaccharidosis type IIIB Co-morbid with Autism Spectrum Disorder.
Published in:
Gazi Medical Journal, 2024, v. 35, p. 6
By:
- Ercan-Şençiçek, A. Gülhan;
- Barak, Tanyeri;
- Rai, Devendra K.;
- Kaymakçalan, Hande;
- Kaya, İlyas;
- Erbilgin, Seda;
- Uytun, Merve Çıkılı;
- Öztop, Didem;
- Gümüş, Hakan;
- Per, Hüseyin;
- Ceylaner, Serdar;
- Aromolaran, Kelly;
- Bozkurt, İçten;
- Mishra-Gorur, Ketu;
- Kontaridis, Maria I.;
- Bilgüvar, Kaya;
- Kılınçaslan, Ayşe;
- Çağlayan, Ahmet Okay;
- Erson-Omay, E. Zeynep;
- Günel, Murat
Publication type:
Article
A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome.
Published in:
2022
By:
- Kaymakçalan, Hande;
- Ercan-Şençiçek, A. Gülhan;
- Cebeci, Ayşe Nurcan;
- Dong, Weilai;
- Yalçın, Ali Seyfi Yalım
Publication type:
Case Study