Heterozygous mutations in and are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly

Author： Hehr Ute   Pineda-Alvarez Daniel   Uyanik Goekhan   Hu Ping   Zhou Nan   Hehr Andreas   Schell-Apacik Chayim   Altus Carola   Daumer-Haas Cornelia   Meiner Annechristin   Steuernagel Peter   Roessler Erich   Winkler Juergen   Muenke Maximilian  

Publisher： Springer Publishing Company

ISSN： 0340-6717

Source： Human Genetics, Vol.127, Iss.5, 2010-05, pp. : 555-561

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