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Journal Article

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

Ute Hehr; Daniel E. Pineda-Alvarez; Goekhan Uyanik; Ping Hu; Nan Zhou; Andreas Hehr; Chayim Schell-Apacik; Carola Altus; Cornelia Daumer-Haas; Annechristin Meiner; Peter Steuernagel; Erich Roessler; Juergen Winkler; Maximilian Muenke
Human Genetics · Vol. 127, Issue 5 · pp. 555-561 · 2010

Abstract

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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2010-05-01
Publication Year2010
Volume127
Issue5
Pages555-561
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-010-0797-4

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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