Süleyman Atar

1PUBLICATIONS
7CO-AUTHORS
Gene and molecular therapy
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Publications (1)

|Nov 11, 2024
Expanding the Genetic and Phenotypic Spectrum of Mowat-Wilson Syndrome: A Study of 10 Turkish Patients With an Intrafamilial Recurrence Caused by First Intragenic Large Deletion.

Ahmet Kablan, Esma Ertürkmen Aru, Süleyman Atar

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Frequent Collaborators

1 joint publications

Ahmet Kablan

1 joint publications

Esma Ertürkmen Aru

1 joint publications

Aydeniz Aydin Gumus

1 joint publications

Ezgi Gökpınar İli