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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

153 related items for PubMed ID: 29770992

  • 1. Holoprosencephaly in the genomics era.
    Roessler E, Hu P, Muenke M.
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):165-174. PubMed ID: 29770992
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  • 5. Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephaly.
    Odent S, Atti-Bitach T, Blayau M, Mathieu M, Aug J, Delezo de AL, Gall JY, Le Marec B, Munnich A, David V, Vekemans M.
    Hum Mol Genet; 1999 Sep; 8(9):1683-9. PubMed ID: 10441331
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  • 10. BOC is a modifier gene in holoprosencephaly.
    Hong M, Srivastava K, Kim S, Allen BL, Leahy DJ, Hu P, Roessler E, Krauss RS, Muenke M.
    Hum Mutat; 2017 Nov; 38(11):1464-1470. PubMed ID: 28677295
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  • 11. ZIC2 in Holoprosencephaly.
    Barratt KS, Arkell RM.
    Adv Exp Med Biol; 2018 Nov; 1046():269-299. PubMed ID: 29442327
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  • 12. Mutations in holoprosencephaly.
    Wallis D, Muenke M.
    Hum Mutat; 2000 Nov; 16(2):99-108. PubMed ID: 10923031
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  • 18. Early pathogenesis of holoprosencephaly.
    Shiota K, Yamada S.
    Am J Med Genet C Semin Med Genet; 2010 Feb 15; 154C(1):22-8. PubMed ID: 20104600
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  • 19. Recent advances in understanding inheritance of holoprosencephaly.
    Dubourg C, Kim A, Watrin E, de Tayrac M, Odent S, David V, Dupé V.
    Am J Med Genet C Semin Med Genet; 2018 Jun 15; 178(2):258-269. PubMed ID: 29785796
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  • 20. Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
    Roessler E, Belloni E, Gaudenz K, Jay P, Berta P, Scherer SW, Tsui LC, Muenke M.
    Nat Genet; 1996 Nov 15; 14(3):357-60. PubMed ID: 8896572
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