Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function (Q36435480)
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Language | Label | Description | Also known as |
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English | Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function |
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Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function (English)
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A R Janecke
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P R Njølstad
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P B Juliusson
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F Lacbawan
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B D Solomon
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E Roessler
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S Domené
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J I Vélez
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N Zhou
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D Hadley
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J Z Balog
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R Long
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A Fryer
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W Smith
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S Omar
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S D McLean
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K Clarkson
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A Lichty
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N J Clegg
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M R Delgado
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E Levey
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E Stashinko
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L Potocki
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M I Vanallen
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J Clayton-Smith
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D Donnai
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D W Bianchi
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H G Brunner
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J C Carey
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U Hehr
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J Müsebeck
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P F Wieacker
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A Postra
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R C M Hennekam
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M-J H van den Boogaard
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A van Haeringen
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A Paulussen
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J Herbergs
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C T R M Schrander-Stumpel
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D Chitayat
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J Hahn
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D M McDonald-McGinn
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E H Zackai
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2 April 2009
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389-398
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Identifiers
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