is a peer-reviewed journal covering all aspects of Human Genetics. It is the official journal of the National Society of Human Genetics The journal was founded in 2012 by Prof. Samia Temtamy, the international pioneer in Human Genetics and limb anomalies, who also was the founder of the Human Genetics and genome Research in National Research Centre, Egypt. The journal is published biannually by the National Society of Human Genetics and Genome Research Institute, National Research Centre, Egypt.
The MEJMG is the first Journal with the aim of collecting together information about genetic diseases and gene mutations in the Middle East region. Publications from different continents of the world are encouraged particularly from Asia and Africa. 
The journal has an outstanding International Editorial Board with extensive academic qualifications, ensuring that the journal maintains high scientific standards and has a broad international coverage. It includes 49 members, specialized professors in different branches of Medical Genetics. They represent several universities in Egypt, Arab Countries, European Countries and USA. Some members are in turn Editors-in-Chief, Associate Editors, and Editorial Advisory Board members of high impact International journals specializing in Medical Genetics.
MEJMG publishes peer-reviewed papers on original investigations in Clinical Genetics, Orodental Genetics, Cytogenetics, Biochemical Genetics, Immunogenetics, Molecular Genetics, and Prenatal Diagnosis. The fields of Clinical and Molecular Dysmorphology are of particular interest. 
Other features include review articles, editorial commentaries, short case reports, and ethical, legal and religious aspects of Human Genome Research and its applications.
MEJMG is supported by the supreme council of universities and has been classified as a highest grade journal.