Literature DB >> 12919141

No evidence of submicroscopic deletion or segmental uniparental disomy within the candidate regions 7p11.2-p13 and 7q31-qter in a series of non-uniparental disomy Silver-Russell syndrome cases.

M Riegel, A Baumer, A Schinzel.   

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Year:  2003        PMID： 12919141     DOI： 10.1034/j.1399-0004.2003.00135.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  1 in total

1.  No evidence for mutations of CTCFL/BORIS in Silver-Russell syndrome patients with IGF2/H19 imprinting control region 1 hypomethylation.

Authors:  Jeremiah Bernier-Latmani; Alessandra Baumer; Phillip Shaw
Journal:  PLoS One       Date:  2009-08-13       Impact factor: 3.240
  1 in total

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