Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia (Q24610890)

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Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
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    Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia (English)
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    William A Paznekas
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    Simeon A Boyadjiev
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    Robert E Shapiro
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    Otto Daniels
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    Catherine E Keegan
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    Jeffrey W Innis
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    Mary Beth Dinulos
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    Cathy Christian
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    Mark C Hannibal
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    February 2003
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    72
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    408-18
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    2
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