Torthaí cuardaigh - Hans Scheffer

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  1. 1
    Stepwise ABC system for classification of any type of genetic variant

    Stepwise ABC system for classification of any type of genetic variant de réir Gunnar Houge, Andreas Laner, Sebahattin Çırak, Nicole de Leeuw, Hans Scheffer, Johan T. den Dunnen

    Foilsithe / Cruthaithe 2021
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  2. 2
    Scanning electron microscopy of a blister roof in dystrophic epidermolysis bullosa

    Scanning electron microscopy of a blister roof in dystrophic epidermolysis bullosa de réir Hiram Larangeira de Almeida, Luciane Maria Alves Monteiro, Ricardo Marques e Silva, Nara Moreira Rocha, Hans Scheffer

    Foilsithe / Cruthaithe 2013
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  3. 3
    Revertant Mosaicism in Epidermolysis Bullosa Caused by Mitotic Gene Conversion

    Revertant Mosaicism in Epidermolysis Bullosa Caused by Mitotic Gene Conversion de réir Marcel F. Jonkman, Hans Scheffer, Rein P. Stulp, Hendri H. Pas, Miranda Nijenhuis, K Heeres, Katsushi Owaribe, Leena Pulkkinen, Jouni Uitto

    Foilsithe / Cruthaithe 1997
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  4. 4
    The Association Between HTR2C Gene Polymorphisms and the Metabolic Syndrome in Patients With Schizophrenia

    The Association Between HTR2C Gene Polymorphisms and the Metabolic Syndrome in Patients With Schizophrenia de réir Hans Mulder, Barbara Franke, Annemarie Aart van der- Beek van der, Johan Arends, Frederik W. Wilmink, Hans Scheffer, Toine C. G. Egberts

    Foilsithe / Cruthaithe 2007
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  5. 5
    Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2

    Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2 de réir Erik‐Jan Kamsteeg, Wolfram Kreß, Claudio Catalli, Jens Michael Hertz, Martina Witsch‐Baumgartner, Michael F. Buckley, Baziel G.M. van Engelen, Marianne Schwartz, Hans Scheffer

    Foilsithe / Cruthaithe 2012
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  6. 6
    The expanding phenotype of<i>POMT1</i>mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardation

    The expanding phenotype of<i>POMT1</i>mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardation de réir Jeroen van Reeuwijk, Svetlana Maugenre, Christa van den Elzen, Aad Verrips, Enrico Bertini, Francesco Muntoni, Luciano Merlini, Hans Scheffer, Han G. Brunner, Pascale Guicheney, Hans van Bokhoven

    Foilsithe / Cruthaithe 2006
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  7. 7
    Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders

    Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders de réir Bart P.C. van de Warrenburg, Meyke Schouten, Susanne T. de Bot, Sascha Vermeer, Rowdy Meijer, Maartje Pennings, Christian Gilissen, Michèl AAP Willemsen, Hans Scheffer, Erik‐Jan Kamsteeg

    Foilsithe / Cruthaithe 2016
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  8. 8
    An association study of 45 folate‐related genes in spina bifida: Involvement of <i>cubilin</i> (<i>CUBN</i>) and <i>tRNA aspartic acid methyltransferase 1</i> (<i>TRDMT1</i>)

    An association study of 45 folate‐related genes in spina bifida: Involvement of <i>cubilin</i> (<i>CUBN</i>) and <i>tRNA aspartic acid methyltransferase 1</i> (<i>TRDMT1</i>) de réir Barbara Franke, Sita H. Vermeulen, Régine P.M. Steegers‐Theunissen, Marieke J. H. Coenen, Mascha M.V.A.P. Schijvenaars, Hans Scheffer, Martin den Heijer, Henk J. Blom

    Foilsithe / Cruthaithe 2009
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  9. 9
    A Cystic Fibrosis Mutation Associated with Mild Lung Disease

    A Cystic Fibrosis Mutation Associated with Mild Lung Disease de réir K. H. Gan, Henk J. Veeze, Ans van den Ouweland, Dicky Halley, Hans Scheffer, Annemieke van der Hout, Shelley E. Overbeek, Johan C. de Jongste, Willem H. Bakker, Harry Heijerman

    Foilsithe / Cruthaithe 1995
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  10. 10
    ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

    ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia de réir Sascha Vermeer, Rowdy Meijer, Benjamin J. Pijl, Janneke Timmermans, J.R.M. Cruysberg, Maaike M. Bos, Helenius J. Schelhaas, Bart P.C. van de Warrenburg, Nine Knoers, Hans Scheffer, B. Kremer

    Foilsithe / Cruthaithe 2008
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  11. 11
    Erratum: Guidelines for diagnostic next-generation sequencing

    Erratum: Guidelines for diagnostic next-generation sequencing de réir Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik A. Sistermans, Marc Sturm, Marjan M. Weiss, Helger G. Yntema, Egbert Bakker, Hans Scheffer, Peter Bauer

    Foilsithe / Cruthaithe 2016
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  12. 12
    Guidelines for diagnostic next-generation sequencing

    Guidelines for diagnostic next-generation sequencing de réir Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik A. Sistermans, Marc Sturm, Marjan M. Weiss, Helger G. Yntema, Egbert Bakker, Hans Scheffer, Peter Bauer

    Foilsithe / Cruthaithe 2015
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  13. 13
    Association of the dopamine transporter (<i>SLC6A3/DAT1</i>) gene 9–6 haplotype with adult ADHD

    Association of the dopamine transporter (<i>SLC6A3/DAT1</i>) gene 9–6 haplotype with adult ADHD de réir Barbara Franke, Martine Hoogman, Alejandro Arias Vásquez, J. G. A. M. Heister, Paul J.M. Savelkoul, Marlies Naber, Hans Scheffer, Lambertus A. Kiemeney, Carol Kan, J. J. Sandra Kooij, Jan K. Buitelaar

    Foilsithe / Cruthaithe 2008
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  14. 14
    Genotype-phenotype correlations in MYCN-related Feingold syndrome

    Genotype-phenotype correlations in MYCN-related Feingold syndrome de réir Carlo Marcelis, Frans A. Hol, Gail E. Graham, Paul N.M.A. Rieu, Richárd Kellermayer, Rowdy Meijer, Dorien Lugtenberg, Hans Scheffer, Hans van Bokhoven, Han G. Brunner, Arjan P.M. de Brouwer

    Foilsithe / Cruthaithe 2008
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  15. 15
    Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders – updated European recommendations

    Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders – updated European recommendations de réir Elisabeth Dequeker, Manfred Stuhrmann, Michael A. Morris, Teresa Casals, Carlo Castellani, Mireille Claustres, Harry Cuppens, Marie des Georges, Claude Férec, Milan Maçek, Pierfranco Pignatti, Hans Scheffer, Marianne Schwartz, Michał Witt, Martin Schwarz, Emmanuelle Girodon

    Foilsithe / Cruthaithe 2008
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  16. 16
    Effects of Keratin 14 Ablation on the Clinical and Cellular Phenotype in a Kindred with Recessive Epidermolysis Bullosa Simplex

    Effects of Keratin 14 Ablation on the Clinical and Cellular Phenotype in a Kindred with Recessive Epidermolysis Bullosa Simplex de réir Marcel F. Jonkman, K Heeres, Hendri H. Pas, Marja J.A. van Luyn, Job D. Elema, Laura D. Corden, Frances J.D. Smith, W.H. Irwin McLean, Frans C. S. Ramaekers, Margaret Burton, Hans Scheffer

    Foilsithe / Cruthaithe 1996
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  17. 17
    Mechanisms of Natural Gene Therapy in Dystrophic Epidermolysis Bullosa

    Mechanisms of Natural Gene Therapy in Dystrophic Epidermolysis Bullosa de réir Dimitra Kiritsi, Marta García, Renske Brander, Cristina Has, Rowdy Meijer, M.J. Escámez, J. Kohlhase, Peter C. van den Akker, Hans Scheffer, Marcel F. Jonkman, Marcela Del Río, Leena Bruckner‐Tuderman, Anna M.G. Pasmooij

    Foilsithe / Cruthaithe 2014
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  18. 18
    Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations

    Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations de réir Susanne T. de Bot, R. T. M. van den Elzen, Arjen R. Mensenkamp, Helenius J. Schelhaas, Michèl A.A.P. Willemsen, Nine V.A.M. Knoers, H.P.H. Kremer, Bart P.C. van de Warrenburg, Hans Scheffer

    Foilsithe / Cruthaithe 2010
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  19. 19
    Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

    Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. de réir Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Heidi Howard, Anne Cambon‐Thomsen, Bartha Maria Knoppers, Hanne Meijers‐Heijboer, Hans Scheffer, Lisbeth Tranebjærg, Wybo Dondorp, Guido M. W. R. de Wert

    Foilsithe / Cruthaithe 2013
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  20. 20
    Whole-genome sequencing in health care

    Whole-genome sequencing in health care de réir Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Heidi Howard, Anne Cambon‐Thomsen, Bartha Maria Knoppers, Hanne Meijers‐Heijboer, Hans Scheffer, Lisbeth Tranebjærg, Wybo Dondorp, Guido M. W. R. de Wert

    Foilsithe / Cruthaithe 2013
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