A. Kablan Et Al. , "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," American Journal of Medical Genetics, Part A , 2024
Kablan, A. Et Al. 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. American Journal of Medical Genetics, Part A .
Kablan, A., Aru, E. E., Atar, S., Gumus, A. A., İli, E. G., KAYHAN, G., ... TEKİN, K.(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. American Journal of Medical Genetics, Part A .
Kablan, Ahmet Et Al. "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," American Journal of Medical Genetics, Part A , 2024
Kablan, Ahmet Et Al. "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." American Journal of Medical Genetics, Part A , 2024
Kablan, A. Et Al. (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." American Journal of Medical Genetics, Part A .
@article{article, author={Ahmet Kablan Et Al. }, title={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}, journal={American Journal of Medical Genetics, Part A}, year=2024}