2011 Group Project 10: Difference between revisions
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== Introduction: What is Duchenne Muscular Dystrophy? == | |||
== History/timeline == | |||
References | == Genetic component == | ||
== Why is it an abnormality - Symptoms effect == | |||
== Diagnosis, future/current prospect (treatments?) == | |||
== 2 case studies == | |||
== Glossary of terms == | |||
== References == | |||
Revision as of 15:33, 31 August 2011
--Mark Hill 12:44, 5 August 2011 (EST) This belongs on your discussion page.
Your Project Goes Here.
2011 Projects: Turner Syndrome | DiGeorge Syndrome | Klinefelter's Syndrome | Huntington's Disease | Fragile X Syndrome | Tetralogy of Fallot | Angelman Syndrome | Friedreich's Ataxia | Williams-Beuren Syndrome | Duchenne Muscular Dystrolphy | Cleft Palate and Lip
