Rett syndrome molecular diagnosis
Selected Abstract
Rett syndrome molecular diagnosis and implications in genetic counseling
Introduction Rett syndrome (RTT [MIM #312750]) is a rare genetic disease with X-linked dominant inheritance. [1] RTT is one of the most frequent causes of mental retardation in females and affects 1/15,000 females worldwide, [2] nearly 1/10000 girls by 12 years of age. Other genetic causes of ... September 1, 2007; Indian Journal of Human Genetics
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Rett syndrome molecular diagnosis and implications in genetic counseling
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