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Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes.

Autor: Wills ES; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands.; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands., Cnossen WR; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands.; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands., Veltman JA; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands., Woestenenk R; Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands., Steehouwer M; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands., Salomon J; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands., Te Morsche RH; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands., Huch M; Wellcome Trust/Cancer Research UK Gurdon Institute, Henry Wellcome Building of Cancer and Developmental Biology, University of Cambridge, Cambridge, UK.; Wellcome Trust/Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, UK.; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK., Hehir-Kwa JY; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands., Banning MJ; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands., Pfundt R; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands., Roepman R; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands., Hoischen A; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands., Drenth JP; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands.; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2016 Dec; Vol. 24 (12), pp. 1707-1714. Date of Electronic Publication: 2016 Aug 24.

ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

Autor: Lugtenberg D; Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands., Yntema HG, Banning MJ, Oudakker AR, Firth HV, Willatt L, Raynaud M, Kleefstra T, Fryns JP, Ropers HH, Chelly J, Moraine C, Gecz J, van Reeuwijk J, Nabuurs SB, de Vries BB, Hamel BC, de Brouwer AP, van Bokhoven H

Publikováno v: American journal of human genetics [Am J Hum Genet] 2006 Feb; Vol. 78 (2), pp. 265-78. Date of Electronic Publication: 2005 Dec 29.

Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation.

Autor: Kleefstra T, Yntema HG, Oudakker AR, Banning MJ, Kalscheuer VM, Chelly J, Moraine C, Ropers HH, Fryns JP, Janssen IM, Sistermans EA, Nillesen WN, de Vries LB, Hamel BC, van Bokhoven H

Publikováno v: Journal of medical genetics [J Med Genet] 2004 May; Vol. 41 (5), pp. 394-9.