Search Results - Ketterling, R.P

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  1. 1
    152 BONE MARROW CONVENTIONAL KARYOTYPING AND FLUORESCENCE IN SITU HYBRIDIZATION (FISH): DEFINING AN EFFECTIVE UTILIZATION STRATEGY FOR THE EVALUATION OF MYELODYSPLASTIC SYNDROME (MDS)

    152 BONE MARROW CONVENTIONAL KARYOTYPING AND FLUORESCENCE IN SITU HYBRIDIZATION (FISH): DEFINING AN EFFECTIVE UTILIZATION STRATEGY FOR THE EVALUATION OF MYELODYSPLASTIC SYNDROME (M... by He, R, Wiktor, A.E, Kurtin, P.J, Van Dyke, D.L, Tefferi, A, Patnaik, M.S, Ketterling, R.P, Hanson, C.A

    Published in Leukemia research
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  2. 2
    Genetic determinants of response and survival in momelotinib-treated patients with myelofibrosis

    Genetic determinants of response and survival in momelotinib-treated patients with myelofibrosis by Pardanani, A, Abdelrahman, R A, Finke, C, Lasho, T T, Begna, K H, Al-Kali, A, Hogan, W J, Litzow, M R, Hanson, C A, Ketterling, R P, Tefferi, A

    Published in Leukemia
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  3. 3
    FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature

    FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature by Pardanani, A., Ketterling, R.P., Li, C.-Y., Patnaik, M.M., Wolanskyj, A.P., Elliott, M.A., Camoriano, J.K., Butterfield, J.H., Dewald, G.W., Tefferi, A.

    Published in Leukemia research
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  4. 4
    DUSP22 AND TP63 REARRANGEMENTS PREDICT OUTCOME OF ALK‐NEGATIVE ANAPLASTIC LARGE CELL LYMPHOMA: A DANISH COHORT STUDY

    DUSP22 AND TP63 REARRANGEMENTS PREDICT OUTCOME OF ALK‐NEGATIVE ANAPLASTIC LARGE CELL LYMPHOMA: A DANISH COHORT STUDY by Pedersen, M.B., Dutoit, S.H., Bendix, K., Ketterling, R.P., Bedroske, P.P., Luoma, I.M., Sattler, C.A., Bennani‐Baiti, N., Noergaard, P., Moeller, M.B., Steiniche, T., d'Amore, F., Feldman, A.

    Published in Hematological oncology
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  5. 5
    Germline origins in the human F9 gene : frequent G:C→A:T mosaicism and increased mutations with advanced maternal age

    Germline origins in the human F9 gene : frequent G:C→A:T mosaicism and increased mutations with advanced maternal age by KETTERLING, R. P, VIELHABER, E, GRUPPO, R, AMBRIZ, R, PAREDES, R, SOMMER, S. S, XUEMIN LI, DROST, J, SCHAID, D. J, KASPER, C. K, PHILLIPS, J. A, KOERPER, M. A, KIM, H, SEXAUER, C

    Published in Human genetics
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  6. 6
    Germ-line origins of mutation in families with hemophilia B : the sex ratio varies with the type of mutation

    Germ-line origins of mutation in families with hemophilia B : the sex ratio varies with the type of mutation by KETTERLING, R. P, VIELHABER, E, BOTTEMA, C. D. K, SCHAID, D. J, COHEN, M. P, SEXAUER, C. L, SOMMER, S. S

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  7. 7
    The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene

    The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene by KETTERLING, R. P, VIELHABER, E, SOMMER, S. S

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  8. 8
    The rates and patterns of deletions in the human factor IX gene

    The rates and patterns of deletions in the human factor IX gene by KETTERLING, R. P, VIELHABER, E. L, LIND, T. J, THORLAND, E. C, SOMMER, S. S

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  9. 9
    Germline origins in the human F9 gene: frequent G:C→A:T mosaicism and increased mutations with advanced maternal age

    Germline origins in the human F9 gene: frequent G:C→A:T mosaicism and increased mutations with advanced maternal age by Ketterling, R.P., Vielhaber, E., Li, X., Drost, J., Schaid, D.J., Kasper, C.K., Phillips III, J.A., Koerper, M.A., Kim, H., Sexauer, C., Gruppo, R., Ambriz, R., Paredes, R., Sommer, S.S.

    Published in Human genetics
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  10. 10
    Recurrent nonsense mutations at arginine residues cause severe hemophilia B in unrelated hemophiliacs

    Recurrent nonsense mutations at arginine residues cause severe hemophilia B in unrelated hemophiliacs by KOEBERL, D. D, BOTTEMA, C. D. K, SARKAR, G, KETTERLING, R. P, CHEN, S.-H, SOMMER, S. S

    Published in Human genetics
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  11. 11
    Hemophilia B in a male with a four-base insertion that arose in the germline of his mother

    Hemophilia B in a male with a four-base insertion that arose in the germline of his mother by BOTTEMA, C. D. K, KETTERLING, R. P, CHO, H. I, SOMMER, S. S

    Published in Nucleic acids research
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  12. 12
    Mutations at arginine residues in two Asian hemophilia B patients

    Mutations at arginine residues in two Asian hemophilia B patients by BOTTEMA, C. D. K, KETTERLING, R. P, KOEBERL, D. D, TAYLOR, S. A, SOMMER, S. S

    Published in Nucleic acids research
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