ŞİMŞEK KİPER, P. Ö. Et Al. 2016. OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey. European Society of Human Genetics Conference 2016 .

ŞİMŞEK KİPER, P. Ö., Taşkıran, E. Z., ARSLAN, U., Koşukçu, C., AKGÜN DOĞAN, Ö., ÜTİNE, G. E., ... ALİKAŞİFOĞLU, A.(2016). OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey . European Society of Human Genetics Conference 2016

ŞİMŞEK KİPER, PELİN Et Al. "OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey," European Society of Human Genetics Conference 2016, 2016

ŞİMŞEK KİPER, PELİN Ö. Et Al. "OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey." European Society of Human Genetics Conference 2016 , 2016

ŞİMŞEK KİPER, P. Ö. Et Al. (2016) . "OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey." European Society of Human Genetics Conference 2016 .

@conferencepaper{conferencepaper, author={PELİN ÖZLEM ŞİMŞEK KİPER Et Al. }, title={OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey}, congress name={European Society of Human Genetics Conference 2016}, city={}, country={}, year={2016}}