Deletions of chromosome 6q are rare and almost all have some form of craniofacial dysmorphisms and structural brain malformations such as corpus callosum agenesis, colpocephaly, polymicrogyria and hydrocephalus. Here we report a preterm infant with cerebellar and pontine hypoplasia as a presentation of terminal deletion of 6q25.

Our Journal of Genetic Disorders & Genetic Reports is an Esteemed, Peer reviewed and Open Access journal which focuses on present latest developments in the field of Mutations & Functional Consequences, Chromosomes, Genes and DNA variations, Environmental genetics, Chromosomal Abnormalities: Incidence & Types, Errors in DNA Repair, Bioinformatics etc. Our journal promulgates all the innovative inventions in the field of Genetic Disorders & Therapeutic Interventions.

Our Editorial Board members are is over whelmed by the response and eagerness of the academic and research contributors to publish with the journal and take part in submissions of the scientific work in the mode of manuscripts. During this year we look forward to taking some initiatives that would encourage and reward our prospective audience which include Chromosomal Abnormalities, Chromosomal Syndromes, Gene Therapy, Genetic Medicine, Medical Genetics.

A standard editorial manager system is utilized for manuscript submission, review, editorial processing and tracking which can be securely accessed by the authors, reviewers and editors for monitoring and tracking the article processing. Manuscripts can be uploaded online or as an email genticsci@eclinicalsci.com

Media Contact :
Jessica Lopez
Editorial office
Journal of Genetic Disorders and Genetic Reports