Redwin Dhas MP

No ORCID on file · 1 paper in corpus · active 2017
2017
Ethiopian journal of health sciences ·doi:10.4314/ejhs.v27i3.14

BackgroundHyperparathyroidism-Jaw Tumor (HPT-JT) syndrome is a rare genetic disorder bearing both a germline and a somatic CDC73 mutation (formerly known as HRPT2), which has been mapped to chromosome 1q25-q31. The association of jaw ossify…