Literature DB >> 12746419

Searching for genomic variants in the MESTIT1 transcript in Silver-Russell syndrome patients.

E Meyer1, H A Wollmann, T Eggermann.   

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Year:  2003        PMID： 12746419      PMCID： PMC1735451          DOI： 10.1136/jmg.40.5.e65

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 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

2.  First genetic screening for maternal uniparental disomy of chromosome 7 in Turkish silver-russell syndrome patients.

Authors:  Emin Karaca; Beyhan Tuysuz; Sacide Pehlivan; Ferda Ozkinay
Journal:  Iran J Pediatr       Date:  2012-12       Impact factor: 0.364

3.  Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution.

Authors:  Layla Parker-Katiraee; Andrew R Carson; Takahiro Yamada; Philippe Arnaud; Robert Feil; Sayeda N Abu-Amero; Gudrun E Moore; Masahiro Kaneda; George H Perry; Anne C Stone; Charles Lee; Makiko Meguro-Horike; Hiroyuki Sasaki; Keiko Kobayashi; Kazuhiko Nakabayashi; Stephen W Scherer
Journal:  PLoS Genet       Date:  2007-03-12       Impact factor: 5.917
  3 in total

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