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    Results: 5

    1.

    Pax genes in embryogenesis and oncogenesis.

    Wang Q, Fang WH, Krupinski J, Kumar S, Slevin M, Kumar P.

    J Cell Mol Med. 2008 Dec;12(6A):2281-94. doi: 10.1111/j.1582-4934.2008.00427.x. Epub 2008 Jul 4. Review.

    PMID:
    18627422
    [PubMed - indexed for MEDLINE]
    2.

    Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?

    Gad A, Laurino M, Maravilla KR, Matsushita M, Raskind WH.

    Am J Med Genet A. 2008 Jul 15;146A(14):1880-5. doi: 10.1002/ajmg.a.32402.

    PMID:
    18553554
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    Craniofacial-deafness-hand syndrome revisited.

    Sommer A, Bartholomew DW.

    Am J Med Genet A. 2003 Nov 15;123A(1):91-4.

    PMID:
    14556253
    [PubMed - indexed for MEDLINE]
    4.

    PAX3 gene structure, alternative splicing and evolution.

    Barber TD, Barber MC, Cloutier TE, Friedman TB.

    Gene. 1999 Sep 17;237(2):311-9.

    PMID:
    10521655
    [PubMed - indexed for MEDLINE]
    5.

    Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome.

    Asher JH Jr, Sommer A, Morell R, Friedman TB.

    Hum Mutat. 1996;7(1):30-5.

    PMID:
    8664898
    [PubMed - indexed for MEDLINE]

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