Jamil A Hashmi

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

Jamil Amjad Hashmi 1 collaboration
Ahmad Almatrafi 1 collaboration
Muhammad Latif 1 collaboration
Abdul Nasir 1 collaboration
Sulman Basit 1 collaboration