(Q28191447)

2

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M Vacca

3

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M D'Esposito

4

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M P Whyte

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

5

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language of work or name

English

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publication date

8 August 2001

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published in

Gene

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volume

273

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issue

2

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page(s)

285-93

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cites work

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A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

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Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E

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Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda

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A novel 16-kilodalton cellular protein physically interacts with and antagonizes the functional activity of c-myc promoter-binding protein 1

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HEREDITARY OSTEOCHONDRODYSTROPHIA DEFORMANS

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Adherence to the first-AUG rule when a second AUG codon follows closely upon the first

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RNA splicing: unexpected spliceosome diversity

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Four evolutionary strata on the human X chromosome.

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Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation

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X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content

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TRAPP, a highly conserved novel complex on the cis-Golgi that mediates vesicle docking and fusion

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