Display Settings:

Format
Sort by

Send to:

Choose Destination

    Results: 3

    1.

    Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome.

    Tassabehji M, Fang ZM, Hilton EN, McGaughran J, Zhao Z, de Bock CE, Howard E, Malass M, Donnai D, Diwan A, Manson FD, Murrell D, Clarke RA.

    Hum Mutat. 2008 Aug;29(8):1017-27.PMID: 18425797 [PubMed - indexed for MEDLINE]Related articles

    2.

    De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophy.

    Hilton EN, Black GC, Manson FD, Schorderet DF, Munier FL.

    Br J Ophthalmol. 2007 Aug;91(8):1083-4. No abstract available. PMID: 17638818 [PubMed - indexed for MEDLINE]Related articles

    3.

    Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination.

    Hilton EN, Manson FD, Urquhart JE, Johnston JJ, Slavotinek AM, Hedera P, Stattin EL, Nordgren A, Biesecker LG, Black GC.

    Hum Mol Genet. 2007 Jul 15;16(14):1773-82. Epub 2007 May 21.PMID: 17517692 [PubMed - indexed for MEDLINE]Related articlesFree article

    Supplemental Content

    Find related data

    Search details

    » See more...