OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey

ŞİMŞEK KİPER P. Ö., Taşkıran E. Z., ARSLAN U., Koşukçu C., AKGÜN DOĞAN Ö., ÜTİNE G. E., ...More

European Society of Human Genetics Conference 2016, 21 - 24 May 2016, (Full Text)

  • Publication Type: Conference Paper / Full Text
  • Hacettepe University Affiliated: Yes