Literature DB >> 15691366

Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver-Russell syndrome patient using methylation-specific PCR assays.

Y Kim, S-S Kim, G Kim, S Park, I S Park, H-W Yoo.   

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Year:  2005        PMID： 15691366     DOI： 10.1111/j.1399-0004.2004.00387.x

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


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  3 in total

1.  Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array.

Authors:  Lili Zhou; Zhaoke Zheng; Yunzhi Xu; Xiaoxiao Lv; Chenyang Xu; Xueqin Xu
Journal:  Mol Cytogenet       Date:  2021-03-19       Impact factor: 2.009

2.  Genomic organization and control of the grb7 gene family.

Authors:  E Lucas-Fernández; I García-Palmero; A Villalobo
Journal:  Curr Genomics       Date:  2008-03       Impact factor: 2.236

Review 3.  [Russell Silver syndrome: report of three cases and review of the literature].

Authors:  Afaf Lamzouri; Ilham Ratbi; Abdelaziz Sefiani
Journal:  Pan Afr Med J       Date:  2013-03-08
  3 in total

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