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• englisch (8)
• deutsch (1)

• Rappold, Gudrun (8)
• Rao, Ercole (4)
• Blaschke, Rüdiger Jörg (3)
• Tröger, Jochen (2)
• Merker, Sabine (2)
• Niesler, Beate (2)
• Wogatzky, Birgit (2)

• Fukami, Maki (2)
• Jauch, Anna (1)
• Kirsch, Stefan (1)
• Bettendorf, Markus (1)
• Heinrich, Udo (1)
• Benes, Vladimir (1)
• Spranger, Stephanie (1)
• Tariverdian, Gholamali (1)
• Rauterberg-Ruland, Inge (1)
• Ansorge, Wilhelm (1)

• Ogata, Tsutomu (2)
• Lindsay, Susan (2)
• Seidel, Jörg (2)
• Clement-Jones, Mark (2)
• Strachan, Tom (2)
• Reinehr, Thomas (1)
• Richter, Alexandra (1)

• Wolff, Kathrin (1)
• Ried, Thomas (1)
• Knoblauch, Hans (1)
• Zumkeller, Walter (1)
• Binder, Gerhard (1)
• Kunze, Jürgen (1)
• Hager, Dieter (1)
• Zintl, Felix (1)
• Claussen, Uwe (1945-2008) (1)
• Orth, Ulrike (1)
• Zeller, Rolf (1)
• Zuniga, Aimée (1)
• Vogt, Susanna (1)
• Robson, Stephen C. (1)
• Muroya, Koji (1)
• Kelbova, Christina (1)
• Glass, Ian (1)
• Drop, Stenvert (1)
• Beensen, Volkmar (1)
• Padilla-Nash, Hesed (1)
• Monaghan, A. Paula (1)
• Vlachopapadoupoulou, Elpis (1)
• Onigata, Kazumichi (1)

Publikationen in heiBIB     

• Rappold, Gudrun: Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature / Gudrun A. Rappold, Maki Fukami, Beate Niesler, Simone Schiller, Walter Zumkeller, Markus Bettendorf,… , 01 March 2002. - 5 S.
  In: The journal of clinical endocrinology & metabolism, ISSN 1945-7197. 87(2002), 3, Seite 1402-1406
  DOI: 10.1210/jcem.87.3.8328
• Wöginger, Simone: Analyse des Homöoboxgens SHOX bei Patienten mit Léri-Weill-Syndrom und Isolierung SHOX-homologer Gene / vorgelegt von Simone Wöginger, 2002. - 120 Bl. : Ill., graph. Darst.
• Seidel, Jörg: Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation / J. Seidel, S. Schiller, C. Kelbova, V. Beensen, U. Orth, S. Vogt, U. Claussen, F. Zintl, G.A. Rappol… , 20 December 2001. - 7 S.
  In: Clinical genetics, ISSN 1399-0004. 59(2001), 2, Seite 115-121
  DOI: 10.1034/j.1399-0004.2001.590209.x
• Fukami, Maki: A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation / Maki Fukami, Stefan Kirsch, Simone Schiller, Alexandra Richter, Vladimir Benes, Brunella Franco, Koj… , 2000 Jul 20. - 11 S.
  In: The American journal of human genetics, ISSN 1537-6605. 67(2000), 3, Seite 563-573
  DOI: 10.1086/303047
• Rappold, Gudrun: The short stature homeobox gene is involved in the skeletal abnormalities in Turner syndrome / G.A. Rappold, R. Blaschke, E. Rao, S. Schiller, M. Clement-Jones, S. Lindsay, T. Strachan, 2000. - 6 S.
  In: Optimizing health care for Turner patients in the 21st century. (2000), Seite 3-8
• Wöginger, Simone: Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome / Simone Schiller, Stephanie Spranger, Birgit Schechinger, Maki Fukami, Sabine Merker, Stenvert LS Dro… , 22 February 2000. - 9 S.
  In: European journal of human genetics, ISSN 1476-5438. 8(2000), 1, Seite 54-62
  DOI: 10.1038/sj.ejhg.5200402
• Clement-Jones, Mark: The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome / Mark Clement-Jones, Simone Schiller, Ercole Rao, Rüdiger J. Blaschke, Aimee Zuniga, Rolf Zeller, Ste… , 22 March 2000. - 8 S.
  In: Human molecular genetics, ISSN 1460-2083. 9(2000), 5, Seite 695-702
  DOI: 10.1093/hmg/9.5.695
• Spranger, Stephanie: Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3 / Stephanie Spranger, Simone Schiller, Anna Jauch, Kathrin Wolff, Inge Rauterberg‐Ruland, Dieter Hager… , 05 April 1999. - 5 S.
  In: American journal of medical genetics, ISSN 1096-8628. 83(1999), 5, Seite 367-371
  DOI: 10.1002/(SICI)1096-8628(19990423)83:5<367::AID-AJMG5>3.0.CO;2-K
• Blaschke, Rüdiger Jörg: SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development / Rüdiger J. Blaschke, A. Paula Monaghan, Simone Schiller, Birgit Schechinger, Ercole Rao, Hesed Padil… , March 3, 1998. - 6 S.
  In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 1091-6490. 95(1998), 5, Seite 2406-2411
  DOI: 10.1073/pnas.95.5.2406

IDs

GND:	1222775409

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Wöginger, Simone in ...

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