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X inactivation of the FMR1 fragile X mental retardation gene.

X chromosome inactivation has been hypothesised to play a role in the aetiology and clinical expression of the fragile X syndrome. The identification of the FMR1 gene involved in fragile X syndrome allows testing of the assumption that the fragile X locus is normally subject to X inactivation. We st...

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Bibliografske podrobnosti
Main Authors: Kirchgessner, C U, Warren, S T, Willard, H F
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051769/
https://ncbi.nlm.nih.gov/pubmed/8825916
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