Resultados da pesquisa - Dilys M. Parry

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  1. 1
    A simplified method of "hypothetical grain" analysis of electron microscope autoradiographs.

    A simplified method of "hypothetical grain" analysis of electron microscope autoradiographs. Por N. M. Blackett, Dilys M. Parry

    Publicado em 1977
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  2. 2
    Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population

    Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population Por Mary L. McMaster, Alisa M. Goldstein, Dilys M. Parry

    Publicado em 2011
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  3. 3
    Neurofibromatosis type 2

    Neurofibromatosis type 2 Por Ashok R. Asthagiri, Dilys M. Parry, John A. Butman, H Jeffrey Kim, Ekaterini Tsilou, Zhengping Zhuang, Russell R. Lonser

    Publicado em 2009
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  4. 4
    T (brachyury) gene duplication confers major susceptibility to familial chordoma

    T (brachyury) gene duplication confers major susceptibility to familial chordoma Por Xiaohong R. Yang, David Ng, David A. Alcorta, Norbert J. Liebsch, Eamonn Sheridan, Sufeng Li, Alisa M. Goldstein, Dilys M. Parry, Michael J. Kelley

    Publicado em 2009
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  5. 5
    Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma.

    Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma. Por Claude Turc‐Carel, Paola Dal Cin, Janusz Limon, Uma Rao, F P Li, Joseph M. Corson, Rebekah Zimmerman, Dilys M. Parry, Janet M. Cowan, A.A. Sandberg

    Publicado em 1987
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  6. 6
    A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

    A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor Por James A. Trofatter, M. MacCollin, Joni L. Rutter, Jill R. Murrell, Mabel P. Duyao, Dilys M. Parry, R Eldridge, Nikolai Kley, Anil G. Menon, K Pulaski

    Publicado em 1993
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  7. 7
    Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

    Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma Por Michael J. Kelley, Jianxin Shi, Bari J. Ballew, Paula L. Hyland, Wenqing Li, Melissa Rotunno, David A. Alcorta, Norbert J. Liebsch, Jason Mitchell, Sara Bass, David A. Roberson, Joseph F. Boland, Michael Cullen, Ji He, Laurie Burdette, Meredith Yeager, Stephen J. Chanock, Dilys M. Parry, Alisa M. Goldstein, Xiaohong R. Yang

    Publicado em 2014
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  8. 8
    Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival

    Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival Por Jiwei Bai, Jianxin Shi, Chuzhong Li, Shuai Wang, Tongwu Zhang, Xing Hua, Bin Zhu, Hela Koka, Ho‐Hsiang Wu, Lei Song, Difei Wang, Mingyi Wang, Weiyin Zhou, Bari J. Ballew, Bin Zhu, Belynda Hicks, Kari G. Rabe, Dilys M. Parry, Yixuan Zhai, Mingxuan Li, Jiang Du, Junmei Wang, Shuheng Zhang, Qian Liu, Peng Zhao, Songbai Gui, Alisa M. Goldstein, Yazhuo Zhang, Xiaohong Yang

    Publicado em 2021
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  9. 9
    Rare germline variants in <i>PALB2</i> and <i>BRCA2</i> in familial and sporadic chordoma

    Rare germline variants in <i>PALB2</i> and <i>BRCA2</i> in familial and sporadic chordoma Por Bing Xia, Kajal Biswas, Tzeh Keong Foo, Thiago T. Gomes, Maximilian Riedel‐Topper, Eileen Southon, Zhihua Kang, Yanying Huo, Susan Reid, Stacey Stauffer, Weiyin Zhou, Bin Zhu, Hela Koka, Sally Yepes, Seth A. Brodie, Kristine Jones, Aurélie Vogt, Bin Zhu, Brian S. Carter, Neal D. Freedman, Belynda Hicks, Meredith Yeager, Stephen J. Chanock, Fergus J. Couch, Dilys M. Parry, Álvaro N.A. Monteiro, Alisa M. Goldstein, Marcelo A. Carvalho, Shyam K. Sharan, Xiaohong R. Yang

    Publicado em 2022
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  10. 10
    Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

    Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene Por Bernd R. Seizinger, Guy A. Rouleau, Laurie J. Ozelius, AH Lane, A.G. Faryniarz, Moses V. Chao, Susan Huson, Bruce R. Korf, Dilys M. Parry, M. A. Pericak‐Vance, Francis S. Collins, Wendy Hobbs, Barbara Falcone, J.A. Iannazzi, Jennie C. L. Roy, Peter St George‐Hyslop, Rudolph E. Tanzi, Mark Bothwell, Meena Upadhyaya, Peter S. Harper, Andrei Goldstein, David L. Hoover, J.L. Bader, M. Anne Spence, John J. Mulvihill, Arthur S. Aylsworth, Jeffery M. Vance, G.O.D. Rossenwasser, P. C. Gaskell, Allen D. Roses, R L Martuza, X. O. Breakefield, James F. Gusella

    Publicado em 1987
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