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Journal Article (231)

  1. 221.
    Journal Article
    Schweiger, S.; Chaoui, R.; Tennstedt, C.; Lehmann, K.; Mundlos, S.; Tinschert, S.: Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review. American Journal of Medical Genetics Part A 120A (4), pp. 547 - 552 (2003)
  2. 222.
    Journal Article
    Morava, É.; Kárteszi, J.; Weisenbach, J.; Caliebe, A.; Mundlos, S.; Méhes, K.: Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. European Journal of Pediatrics 161 (11), pp. 619 - 622 (2002)
  3. 223.
    Journal Article
    Unger, S.; Mornet, E.; Mundlos, S.; Blaser, S.; Cole, D. E.: Severe cleidocranial dysplasia can mimic hypophosphatasia. European Journal of Pediatrics 161 (11), pp. 623 - 626 (2002)
  4. 224.
    Journal Article
    Sander, T.; Toliat, M. R.; Heils, A.; Leschik, G.; Becker, C.; Rüschendorf, F.; Rohde, K.; Mundlos, S.; Nürnberg, P.: Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy. Epilepsy Research 51 (3), pp. 249 - 255 (2002)
  5. 225.
    Journal Article
    Stricker, S.; Fundele, R.; Vortkamp, A.; Mundlos, S.: Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 245 (1), pp. 95 - 108 (2002)
  6. 226.
    Journal Article
    Stricker, S.; Fundele, R.; Vortkamp, A.; Mundlos, S.: Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 245 (1), pp. 95 - 108 (2002)
  7. 227.
    Journal Article
    Stricker, S.; Fundele, R.; Vortkamp, A.; Mundlos, S.: Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 245 (1), pp. 95 - 108 (2002)
  8. 228.
    Journal Article
    Kalache, K. D.; Lehmann, K.; Chaoui, R.; Kivelitz, D. E.; Mundlos, S.; Bollmann, R.: Prenatal diagnosis of partial agenesis of the corpus callosum in a fetus with thanatophoric dysplasia type 2. Prenatal Diagnosis 22 (5), pp. 404 - 407 (2002)
  9. 229.
    Journal Article
    Otto, F.; Kanegane, H.; Mundlos, S.: Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. Human Mutation 19 (3), pp. 209 - 216 (2002)
  10. 230.
    Journal Article
    Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), pp. 53 - 67 (2002)
  11. 231.
    Journal Article
    Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), pp. 53 - 67 (2002)

Book (1)

  1. 232.
    Book
    Mundlos, S.; Horn, D.: Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 pp.

Conference Paper (1)

  1. 233.
    Conference Paper
    Schöpflin, R.; Andrey, G.; Heinrich, V.; Franke, M.; Ibrahim, D.; Paliou, C.; Mundlos, S.; Vingron, M.: Identification of potential regulatory elements in Capture-C interaction profiles. In: Genome Regulation in 3D. Genome Regulation in 3D, Rehovot, Israel, June 28, 2015 - June 30, 2015. Weizmann Institute, Rehovot, Israel (2015)

Other (1)

  1. 234.
    Other
    Despang, A.; Schöpflin, R.; Franke, M.; Ali, S.; Jerkovic, I.; Paliou, C.; Chan, W.-L.; Timmermann, B.; Wittler, L.; Vingron, M. et al.; Mundlos, S.; Ibrahim, D. M.: Functional dissection of TADs reveals non-essential and instructive roles in regulating gene expression, (2019)
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