Segregation analysis of the X-chromosome in a family with rett syndrome in two generations
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference15 articles.
1. Abnormal mitochondria in the Rett syndrome
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1. Letters To The Editor;Developmental Medicine & Child Neurology;2008-11-12
2. Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother;Clinical Genetics;2008-06-28
3. Rett syndrome: potential gene sources - phenotypical variability;Clinical Genetics;2008-06-28
4. Rett syndrome: random X chromosome inactivation;Clinical Genetics;2008-06-28
5. Neither uniparental disomy nor skewed X-inactivation explains Rett syndrome;Clinical Genetics;2008-04-23
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