Search Results - Radak, Amy L.

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  1. 1
    Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility

    Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility by CUSHMAN, Lisa J, WATKINS-CHOW, Dawn E, BRINKMEIER, Michelle L, RAETZMAN, Lori T, RADAK, Amy L, LLOYD, Ricardo V, CAMPER, Sally A

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  2. 2
    X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15

    X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15 by Demirci, F. Yesim K., Rigatti, Brian W., Wen, Gaiping, Radak, Amy L., Mah, Tammy S., Baic, Corrine L., Traboulsi, Elias I., Alitalo, Tiina, Ramser, Juliane, Gorin, Michael B.

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  3. 3
    Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15

    Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15 by Demirci, F. Yesim K., Gupta, Nisha, Radak, Amy L., Rigatti, Brian W., Mah, Tammy S., Milam, Ann H., Gorin, Michael B.

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  4. 4
    A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping

    A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping by Demirci, F.Yesim K., Radak, Amy L., Rigatti, Brian W., Mah, Tammy S., Gorin, Michael B.

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  5. 5
    A presumed missense mutation ofRPGRcauses abnormal RNA splicing with exon skipping

    A presumed missense mutation ofRPGRcauses abnormal RNA splicing with exon skipping by Demirci, FYesim K, Radak, Amy L, Rigatti, Brian W, Mah, Tammy S, Gorin, Michael B

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  6. 6
    Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in theRPGRexon ORF15

    Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in theRPGRexon ORF15 by Demirci, F Yesim K, Gupta, Nisha, Radak, Amy L, Rigatti, Brian W, Mah, Tammy S, Milam, Ann H, Gorin, Michael B

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