Ceren Yılmaz Uzman
3PUBLICATIONS
10CO-AUTHORS

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Publications (3)
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|Jun 19, 2023
A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndrome.Ceren Yılmaz Uzman, Semra Gürsoy, Filiz Hazan
|Jun 07, 2023
Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single center.Mehmet Kocabey, Hande Özkalaycı, Tufan Çankaya
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Frequent Collaborators
2 joint publications
Semra Gürsoy
2 joint publications
Filiz Hazan
1 joint publications
Mehmet Kocabey
1 joint publications
Hande Özkalaycı
1 joint publications
Özge Köprülü
1 joint publications
Sezer Acar
1 joint publications
İbrahim Mert Erbaş
1 joint publications
Özlem Nalbantoğlu
1 joint publications
Hüseyin Anıl Korkmaz
1 joint publications
Behzat Özkan