SciTechnol http://www.scitechnol.com/ SciTechnol is an international, multidisciplinary organization dedicated to pure scientific research and scientific dissemination. It promotes awareness to all arenas of public to encourage research and aid scientific community by executing the significance of latest research. SciTechnol also provides a common platform for interdisciplinary exchange of ideas and information globally. http://www.scitechnol.com/ArchiveJGDGR/currentissue-genetic-disorders-genetic-reports.php Journal of Genetic Disorders & Genetic Reports Volume 5, Issue 4 http://www.scitechnol.com/peer-review/chromosome-22q112-and-7q1123-microdeletions-in-children-with-congenital-heart-defects-detected-by-fish-technique-zEu8.php?article_id=5669 Chromosome 22q112 and 7q1123 Microdeletions in Children with Congenital Heart Defects Detected by Fish Technique Mirea AM, Popp RA, Lazea C, Cuzmici Z, Al Khzouz C, Bucerzan S, Nascu, Man S, Iurian S, Miclea DL http://www.scitechnol.com/peer-review/treatment-with-agalsidase-alfa-during-pregnancy-in-a-heterozygous-female-withfabry-disease-W3mV.php?article_id=5317 Treatment with Agalsidase Alfa during Pregnancy in a Heterozygous Female with Fabry Disease Antonio Pisani, Giuseppe Bifulco, Attilio Di Spiezio Sardo and Eleonora Riccio http://www.scitechnol.com/peer-review/screening-of-genetic-mutations-in-gba1-gigyf2-and-vps35-in-parkinson-disease-patients-from-india-Oe1F.php?article_id=5442 Screening of Genetic Mutations in GBA1 GIGYF2 and VPS35 in Parkinson Disease Patients from India Tamali Halder, Janak Raj, Sharad Pandey, Ajay Kumar, Sagar Kawale, Sandeep Chaudhary, Vivek Sharma, Deepika Joshi and Parimal Das http://www.scitechnol.com/peer-review/smithmagenis-syndrome-treated-with-ramelteon-and-amphetaminedextroamphetamine-case-report-and-review-of-the-literature-29KH.php?article_id=5521 SmithMagenis Syndrome Treated with Ramelteon and Amphetaminedextroamphetamine Case Report and Review of the Literature Baek WS, Elsea SH http://www.scitechnol.com/peer-review/same-mutation-in-two-patients-with-mucopolysaccharidosis-type-vi-maroteauxlamy-syndrome-coming-from-different-municipalities-in-th-4dkb.php?article_id=5653 Same Mutation in Two Patients with Mucopolysaccharidosis Type VI MaroteauxLamy Syndrome Coming from Different Municipalities in the Department of Cauca Southwestern Colombia Acosta MA, Lago RM, Barros F and Carracedo AM