Open AccessClinical Utility of Whole Genome Sequencing for Undiagnosed Rare Genetic Disorders
Author(s) -
Muhammad Qasim Awan
Publication year - 2021
Publication title -
jlumhs
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.13
H-Index - 12
eISSN - 2309-8627
pISSN - 1729-0341
DOI - 10.22442/jlumhs.2021.00872
Subject(s) - medicine , whole genome sequencing , genetic diagnosis , dna sequencing , computational biology , genome , genetics , gene , biology