Fragile X Syndrome. What is Fragile X? Fragile X, also known as Martin-Bell syndrome, is an X-linked genetic Fragile X, also known as Martin-Bell syndrome,
What is Cytoplasm. Cytoplasm Jelly-like fluid Occupies space Structure Cytosol –Cytoskeleton filament –Organic molecules –Salt & water.
DNA Profiling Field Trip 411. Basics Nucleus contains 23 pairs of chromosomes. Each chromosome contains alleles or versions of traits (ex: eye color,
Coping with Changing Controlled Vocabularies James J. Cimino, M.D. Paul D. Clayton, Ph.D. Department of Medical Informatics Columbia University.
Software for Merging Microsatellite Datasets Angela Presson 2 Jeanette Papp 1 Eric Sobel 1 Ken Lange 1,2,3 1. Department of Human Genetics 2. Department.
GENETIC DISORDERS. Marfan syndrome Ehlers-Danlos syndrome Familial hypercholesterolemia. Alkaptonuria Turnes syndrome Neurofibromatosis.
©2012 Cengage Learning. All Rights Reserved. Chapter 5 Developmental Disabilities: Causes and Classifications.
Fragile What? – An Overview of Fragile X Syndrome and its Associated Disorders Matt Rhodes Parent Contact - LINKS Leader Fragile X Association of Alabama.
