Pages that link to "Q33596633"
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The following pages link to Male Rett syndrome variant: application of diagnostic criteria (Q33596633):
Displaying 15 items.
- Identification of MeCP2 mutations in a series of females with autistic disorder (Q28207072) (← links)
- Rett syndrome: a prototypical neurodevelopmental disorder (Q28255289) (← links)
- The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome (Q34733514) (← links)
- Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype (Q34733527) (← links)
- Rapid genotyping of common MeCP2 mutations with an electronic DNA microchip using serial differential hybridization (Q35870262) (← links)
- Deciphering Rett syndrome with mouse genetics, epigenomics, and human neurons (Q37629987) (← links)
- MeCP2-Related Diseases and Animal Models (Q37632847) (← links)
- Microglia as modulators of cognition and neuropsychiatric disorders (Q38022207) (← links)
- Rett syndrome and MeCP2. (Q38194967) (← links)
- Brief report: systematic review of Rett syndrome in males (Q38562939) (← links)
- Rett syndrome: clinical manifestations in males with MECP2 mutations (Q48650852) (← links)
- Occurrence of Rett syndrome in boys (Q48856336) (← links)
- Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling. (Q51958928) (← links)
- Transcriptome level analysis in Rett syndrome using human samples from different tissues. (Q55654628) (← links)
- Animal Models of Epigenetic Regulation in Neuropsychiatric Disorders (Q83172838) (← links)