Hasil Pencarian - Hennie T. Bruggenwirth

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  1. 1
    Genome-wide methylation analysis in patients with proximal hypospadias – a pilot study and review of the literature

    Genome-wide methylation analysis in patients with proximal hypospadias – a pilot study and review of the literature oleh Yolande van Bever, Ruben G Boers, Hennie T Brüggenwirth, Wilfred Fj van IJcken, Frank J Magielsen, Annelies de Klein, Joachim B Boers, Leendert Hj Looijenga, Erwin Brosens, Joost Gribnau, Sabine E Hannema

    Diterbitkan 2024-12-01
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  2. 2
    Application of the New Classification on Patients with a Disorder of Sex Development in Indonesia

    Application of the New Classification on Patients with a Disorder of Sex Development in Indonesia oleh A. Zulfa Juniarto, Yvonne G. van der Zwan, Ardy Santosa, Remko Hersmus, Frank H. de Jong, Renske Olmer, Hennie T. Bruggenwirth, Axel P. N. Themmen, Katja P. Wolffenbuttel, Leendert H. J. Looijenga, Sultana M. H. Faradz, Stenvert L. S. Drop

    Diterbitkan 2012-01-01
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  3. 3
    A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.

    A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation. oleh Remko Hersmus, Yvonne G van der Zwan, Hans Stoop, Pascal Bernard, Rajini Sreenivasan, J Wolter Oosterhuis, Hennie T Brüggenwirth, Suzan de Boer, Stefan White, Katja P Wolffenbuttel, Marielle Alders, Kenneth McElreavy, Stenvert L S Drop, Vincent R Harley, Leendert H J Looijenga

    Diterbitkan 2012-01-01
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  4. 4
    Multi-Omics Profiling in Marfan Syndrome: Further Insights into the Molecular Mechanisms Involved in Aortic Disease

    Multi-Omics Profiling in Marfan Syndrome: Further Insights into the Molecular Mechanisms Involved in Aortic Disease oleh Judith M. A. Verhagen, Joyce Burger, Jos A. Bekkers, Alexander T. den Dekker, Jan H. von der Thüsen, Marina Zajec, Hennie T. Brüggenwirth, Marianne L. T. van der Sterre, Myrthe van den Born, Theo M. Luider, Wilfred F. J. van IJcken, Marja W. Wessels, Jeroen Essers, Jolien W. Roos-Hesselink, Ingrid van der Pluijm, Ingrid M. B. H. van de Laar, Erwin Brosens

    Diterbitkan 2021-12-01
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  5. 5
    The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres

    The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres oleh Luca Persani, Martine Cools, Stamatina Ioakim, S Faisal Ahmed, Silvia Andonova, Magdalena Avbelj-Stefanija, Federico Baronio, Jerome Bouligand, Hennie T Bruggenwirth, Justin H Davies, Elfride De Baere, Iveta Dzivite-Krisane, Paula Fernandez-Alvarez, Alexander Gheldof, Claudia Giavoli, Claus H Gravholt, Olaf Hiort, Paul-Martin Holterhus, Anders Juul, Csilla Krausz, Kristina Lagerstedt-Robinson, Ruth McGowan, Uta Neumann, Antonio Novelli, Xavier Peyrassol, Leonidas A Phylactou, Julia Rohayem, Philippe Touraine, Dineke Westra, Valeria Vezzoli, Raffaella Rossetti

    Diterbitkan 2022-11-01
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  6. 6
    Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge

    Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge oleh Erwin Brosens, Nina C. J. Peters, Kim S. van Weelden, Kim S. van Weelden, Kim S. van Weelden, Charlotte Bendixen, Rutger W. W. Brouwer, Rutger W. W. Brouwer, Frank Sleutels, Hennie T. Bruggenwirth, Wilfred F. J. van Ijcken, Wilfred F. J. van Ijcken, Danielle C. M. Veenma, Danielle C. M. Veenma, Suzan C. M. Cochius-Den Otter, Rene M. H. Wijnen, Alex J. Eggink, Marieke F. van Dooren, Heiko Martin Reutter, Heiko Martin Reutter, Robbert J. Rottier, Robbert J. Rottier, J. Marco Schnater, Dick Tibboel, Annelies de Klein

    Diterbitkan 2022-02-01
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