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    Am J Med Genet. 1993 Oct 1;47(5):637-9.

    Saethre-Chotzen syndrome with familial translocation at chromosome 7p22.

    Reid CS, McMorrow LE, McDonald-McGinn DM, Grace KJ, Ramos FJ, Zackai EH, Cohen MM Jr, Jabs EW.

    Division of Pediatric Genetics, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Camden.

    Chromosome analysis of a male infant and his mother with Saethre-Chotzen syndrome demonstrated an apparently balanced translocation, t(2;7)(p23;p22). This association lends support to localization of the gene for Saethre-Chotzen syndrome to the 7p2 region and supports further involvement of gene(s) in the 7p22 region.

    PMID: 8266989 [PubMed - indexed for MEDLINE]

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