
Mutation Analysis of MSX1 in Pakistani Population
Pierre Robin Sequence and Non Syndromic Cleft Lip and/or Palate (Orofacial Cleft)
LAP Lambert Academic Publishing
Published on 20. June 2014
Book
Paperback/Softback
72 pages
978-3-659-55625-8 (ISBN)
Description
Genetic defects are very common in every population such as orofacial clefts that affect the normal facial anatomy. MSX1 is one of the genes controlling the facial features. This book will be helpful for the students who are just starting their Genetic studies at basic level. More over this book has various protocols involved in molecular examinations including DNA Isolation, Primer designing, Polymerase Chain Reaction and introduction of various elution kits. Students can also go through different bioinformatics tools involved in mutation analysis. In addition you can find some information on basic structures responsible for normal facial development. This study was conducted for the mutation analysis of MSX1 that comprised of two exons. The part we evaluated was not actually responsible for the clefts in our sample population. But mutations in this gene (MSX1) has played critical roles in some other populations which is very obviously reported by different scientists throughout the world.
More details
Language
English
Product notice
Paperback (trade)
Unsewn / adhesive bound
Dimensions
Height: 220 mm
Width: 150 mm
Thickness: 5 mm
Weight
125 gr
ISBN-13
978-3-659-55625-8 (9783659556258)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Persons
Waqas Ahmad. MS Scholar, Forensic Chemistery, Government College and University Lahore, Pakistan. He did his BS(Hons.) in Microbiology and Molecular Genetics in University of the Punjab, Lahore , Pakistan. Working at Punjab Forensic Science Agency, DNA and Serology Department , Lahore, Pakistan.