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  • Holoprosencephaly
  • Chiari malformation
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    		Citation
    12002Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.



    		+-nlAm J Hum Genet 71(5):1017-32 (2002)
    22009Pathogenesis of holoprosencephaly.



    		+-nlJ Clin Invest 119(6):1403-13 (2009)
    32007Holoprosencephaly.



    		+-nlOrphanet J Rare Dis 2(-):8 (2007)
    42000Assessment of the deep gray nuclei in holoprosencephaly.



    		+-nlAJNR Am J Neuroradiol 21(10):1955-61 (2000)
    51999Coexistent holoprosencephaly and Chiari II malformation.



    		+-nlAJNR Am J Neuroradiol 20(9):1678-81 (1999)
    62010Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):176-82 (2010)
    72010The molecular genetics of holoprosencephaly.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):52-61 (2010)
    82010Genesis of teratogen-induced holoprosencephaly in mice.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):29-42 (2010)
    92010Roles of bone morphogenetic protein signaling and its antagonism in holoprosencephaly.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):43-51 (2010)
    102010Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):93-101 (2010)
    112010Analysis of genotype-phenotype correlations in human holoprosencephaly.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):133-41 (2010)
    122010Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literature.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):170-5 (2010)
    132010Holoprosencephaly due to numeric chromosome abnormalities.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):146-8 (2010)
    142010Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature.



    		+-nlAm J Med Genet C Semin Med Genet 154C(1):158-69 (2010)



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