Segmental duplication associated with the human-specific inversion of chromosome 18: a further example of the impact of segmental duplications on karyotype and genome evolution in primates

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Springer Publishing Company

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Rothmund–Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene

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Molecular Genetics & Genomic Medicine, Vol. 4, Iss. 3, 2016-05 ,pp. : 359-366

John Wiley & Sons Inc

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The genomic structure of C14orf1 is conserved across eukarya

By Ottolenghi Chris   Daizadeh Iraj   Ju Albert   Kossida Sophia   Renault Georges   Jacquet Michel   Fellous Arlette   Gilbert Walter   Veitia Reiner  

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Specific interaction between the XNP / ATR-X gene product and the SET domain of the human EZH2 protein

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Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL

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