INTEGRATED CLINICAL AND GENETIC APPROACH FOR DIAGNOSIS OF RETT SYNDROME IN CHILDREN
Rett syndrome represents one of the most important neuropsychiatric genetic diseases. It affects generally girls with the incidence 1:10000-1:15000. Mutations in clinked gene mecp2 are considered as the main cause of the disease. The particular patterns of chromosome x replication (type C) are obser...
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| Principais autores: | , , , , |
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| Formato: | Livro |
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"Paediatrician" Publishers LLC,
2007-07-01T00:00:00Z.
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| Número de Chamada: |
A1234.567 |
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