INTEGRATED CLINICAL AND GENETIC APPROACH FOR DIAGNOSIS OF RETT SYNDROME IN CHILDREN
<em>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)...
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| Formaat: | Boek |
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"Paediatrician" Publishers LLC,
2007-01-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |