Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly (Q33911957)

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Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly
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    Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly (English)
    Daniel E Pineda-Alvarez
    Goekhan Uyanik
    Andreas Hehr
    Chayim Schell-Apacik
    Carola Altus
    Cornelia Daumer-Haas
    Annechristin Meiner
    Peter Steuernagel
    Erich Roessler
    Juergen Winkler
    Maximilian Muenke
    16 February 2010

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