2011 Group Project 3: Difference between revisions

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==Epidemiology==
==Epidemiology==
[[File:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2889887/table/T1/|thumb|Details regarding all men diagnosed with a karyotype compatible with 47,XYY in Denmark during 1965 to 2008.]]
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


==Signs and Symptoms==
==Signs and Symptoms==

Revision as of 09:52, 13 August 2011

Note - This page is an undergraduate science embryology student group project 2011.
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



Kleinfelter Syndrome

Introduction

History

Epidemiology

Signs and Symptoms

Etiology

Pathogenesis

Other Similar Defects

Glossary

References


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

Retrieved from ‘https://embryology.med.unsw.edu.au/embryology/index.php?title=2011_Group_Project_3&oldid=62807’
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