Published 2000
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MECP2 Mutations and Rett Syndrome Phenotypes
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Abstract
Seventy-one sporadic and 7 familial Rett syndrome (RTT) patients were screened for MECP2 mutations by direct sequencing and the pattern of X chromosome inactivation (XCI) was determined in 39 RTT patients at the Baylor College of Medicine, Houston, TX.Files
PNB-14-39-a.pdf
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- PNB-14-39-a
Dates
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2000When the item was originally created.