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Olmer, R.
( R. Olmer)
x syndrome mutation fmr 1 gene syndrome sister genet fmrp expression x chromosome female article oostra ba oostra avected monozygotic retardation expression willemsen hair roots chromosome avected sister galjaard h x inactivation pattern hagerman rj monozygotic twins inactivation hair root analysis x mutation fmr 1 allele allele willemsen r phenotype otero diverent brain analysis mandel jl taylor ak olmer blood diego otero nelson dl pieretti m x inactivation function prognostic indicator number oberle i warren st study avected females result denckla mb monozygous twins caskey ct renske olmer correlation diego otero y 30 march 2000 development diego protein breakpoint cluster region neurone taylor fmr 1 protein lyonisation fmr 1 alleles methylation jmg.bmj.com genetic phosphatase immunolabelling technique sanchez van ommen gjb 20 hair roots panel november downloaded 29 november 2006 pattern capacity
1 Most Recent Publications
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Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype
(Article)
Willemsen, R. Olmer, R. Diego Otero, Y. de Oostra, B.A. |
2000-01-01
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