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
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| (P356) |
10.1086/504440
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| (P698) |
16685650
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1474108
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7094879
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release_zfarpy7npndo5kvicxwxbkcpta
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