Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosis (Q56770882)

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Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosis
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    Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosis (English)
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    Dina J Zand
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    Laurie Demmer
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    Carol E Anderson
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    Elaine H Zackai
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    Elizabeth Denenberg
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    Kim Jenny
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    Deborah L Stabley
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    Katia Sol-Church
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    October 2013
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    161A
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    10
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    2420-30
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