Search Results - Coats, Caraline

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  1. 1
    Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration

    Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration by Swain, P K, Chen, S, Wang, Q L, Affatigato, L M, Coats, C L, Brady, K D, Fishman, G A, Jacobson, S G, Swaroop, A, Stone, E, Sieving, P A, Zack, D J

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    Leber Congenital Amaurosis Caused by a Homozygous Mutation (R90W) in the Homeodomain of the Retinal Transcription Factor CRX: Direct Evidence for the Involvement of CRX in the Development of Photoreceptor Function

    Leber Congenital Amaurosis Caused by a Homozygous Mutation (R90W) in the Homeodomain of the Retinal Transcription Factor CRX: Direct Evidence for the Involvement of CRX in the Deve... by Swaroop, Anand, Wang, Qing-Liang, Wu, Weiping, Cook, Jason, Coats, Caraline, Xu, Siqun, Chen, Shiming, Zack, Donald J., Sieving, Paul A.

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    Functional Implications of the Spectrum of Mutations Found in 234 Cases With X-linked Juvenile Retinoschisis (XLRS)

    Functional Implications of the Spectrum of Mutations Found in 234 Cases With X-linked Juvenile Retinoschisis (XLRS) by The Retinoschisis Consortium

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    Small physician practices can continue to thrive through closer relationships with their payers

    Small physician practices can continue to thrive through closer relationships with their payers by Coats, Caraline

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