Jamil Amjad Hashmi

Affiliations
  • Center for Genetics and Inherited Diseases, Taibah University, Almadinah Almunawwarah, Saudi Arabia.

Publications (1)

An 18 bps in-frame deletion mutation in RUNX2 gene is a population polymorphism rather than a pathogenic variant.

European journal of medical genetics
Avec: Jamil Amjad Hashmi , Ahmad Almatrafi , Muhammad Latif , Abdul Nasir , Sulman Basit

Réseau de co-auteurs

Ahmad Almatrafi 1 collaboration
Muhammad Latif 1 collaboration
Abdul Nasir 1 collaboration
Sulman Basit 1 collaboration