Hasil Pencarian - Daniel Groepper

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  1. 1
    P281: Atypical maternally inherited CDKN1C variant causing IMAGe syndrome in a newborn

    P281: Atypical maternally inherited CDKN1C variant causing IMAGe syndrome in a newborn oleh Daniel Groepper, Julie Fleischer, Jacqueline Lyman

    Diterbitkan 2024-01-01
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  2. 2
    P110: Case report of APC promoter 1B deletion associated with classic FAP

    P110: Case report of APC promoter 1B deletion associated with classic FAP oleh Mary O'Connor, Daniel Groepper, Julie Fleischer

    Diterbitkan 2024-01-01
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  3. 3
    P342: Broadening the phenotype of ABL1-associated disorder

    P342: Broadening the phenotype of ABL1-associated disorder oleh Christopher Vincent, Daniel Groepper, Lamya Mubayed, Julie Fleischer

    Diterbitkan 2023-01-01
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  4. 4
    P239: Mosaic trisomy 17 and tetraploidy: A case report

    P239: Mosaic trisomy 17 and tetraploidy: A case report oleh Zach Ryder, Daniel Groepper, Fiyinfoluwa Soluade, Henry Adekola, Morgan Schriever, Julie Fleischer

    Diterbitkan 2024-01-01
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  5. 5
    Pharmacokinetic modeling of an induction regimen for in vivo combined testing of novel drugs against pediatric acute lymphoblastic leukemia xenografts.

    Pharmacokinetic modeling of an induction regimen for in vivo combined testing of novel drugs against pediatric acute lymphoblastic leukemia xenografts. oleh Barbara Szymanska, Urszula Wilczynska-Kalak, Min H Kang, Natalia L M Liem, Hernan Carol, Ingrid Boehm, Daniel Groepper, C Patrick Reynolds, Clinton F Stewart, Richard B Lock

    Diterbitkan 2012-01-01
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  6. 6
    Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome.

    Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome. oleh Sarah R Poll, Renan Martin, Elizabeth Wohler, Elizabeth S Partan, Elizabeth Walek, Shaima Salman, Daniel Groepper, Lisa Kratz, Mirlene Cernach, Reynaldo Jesus-Garcia, Chad Haldeman-Englert, Yoon Jae Choi, Carol D Morris, Bernard Cohen, Julie Hoover-Fong, David Valle, Gregg L Semenza, Nara L M Sobreira

    Diterbitkan 2022-12-01
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  7. 7
    Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

    Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders oleh Ilaria Mannucci, Nghi D. P. Dang, Hannes Huber, Jaclyn B. Murry, Jeff Abramson, Thorsten Althoff, Siddharth Banka, Gareth Baynam, David Bearden, Ana Beleza-Meireles, Paul J. Benke, Siren Berland, Tatjana Bierhals, Frederic Bilan, Laurence A. Bindoff, Geir Julius Braathen, Øyvind L. Busk, Jirat Chenbhanich, Jonas Denecke, Luis F. Escobar, Caroline Estes, Julie Fleischer, Daniel Groepper, Charlotte A. Haaxma, Maja Hempel, Yolanda Holler-Managan, Gunnar Houge, Adam Jackson, Laura Kellogg, Boris Keren, Catherine Kiraly-Borri, Cornelia Kraus, Christian Kubisch, Gwenael Le Guyader, Ulf W. Ljungblad, Leslie Manace Brenman, Julian A. Martinez-Agosto, Matthew Might, David T. Miller, Kelly Q. Minks, Billur Moghaddam, Caroline Nava, Stanley F. Nelson, John M. Parant, Trine Prescott, Farrah Rajabi, Hanitra Randrianaivo, Simone F. Reiter, Janneke Schuurs-Hoeijmakers, Perry B. Shieh, Anne Slavotinek, Sarah Smithson, Alexander P. A. Stegmann, Kinga Tomczak, Kristian Tveten, Jun Wang, Jordan H. Whitlock, Christiane Zweier, Kirsty McWalter, Jane Juusola, Fabiola Quintero-Rivera, Utz Fischer, Nan Cher Yeo, Hans-Jürgen Kreienkamp, Davor Lessel

    Diterbitkan 2021-05-01
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