The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males (Q24546616)

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The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males
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    The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males (English)
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    Stephen R F Twigg
    1 reference
    Kazuya Matsumoto
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    Alexa M J Kidd
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    Indira B Taylor
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    Richard B Fisher
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    A Jeannette M Hoogeboom
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    Irene M J Mathijssen
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    M Teresa Lourenco
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    Jenny E V Morton
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    Elizabeth Sweeney
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    Louise C Wilson
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    John B Mulliken
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    Steven A Wall
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    June 2006
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    78
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    6
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    999-1010
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