Journal Article (356)

  1. 341.
    Journal Article
    Borthwick, K. J.; Kandemir, N.; Topaloglu, R.; Kornak, U.; Bakkaloglu, A.; Yordam, N.; Ozen, S.; Mocan, H.; Shah, G. N.; Sly, W. S. et al.; Karet, F. E.: A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis. Journal of Medical Genetics 40 (2), pp. 115 - 121 (2003)
  2. 342.
    Journal Article
    Shultz, L. D.; Lyons, B. L.; Burzenski, L. M.; Gott, B.; Samuels, R.; Schweitzer, P. A.; Dreger, C.; Herrmann, H.; Kalscheuer, V.; Olins, A. L. et al.; Olins, D. E.; Sperling, K.; Hoffmann, K.: Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly. Human Molecular Genetics 12 (1), pp. 61 - 69 (2003)
  3. 343.
    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)
  4. 344.
    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)
  5. 345.
    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)
  6. 346.
    Journal Article
    Katzke, S.; Booms, P.; Tiecke, F.; Palz, M.; Pletschacher, A.; Türkmen, S.; Neumann, L. M.; Pregla, R.; Leitner, C.; Schramm, C. et al.; Lorenz, P.; Hagemeier, C.; Fuchs, J.; Skovby, F.; Rosenberg, T.; Robinson, P. N.: TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies. Human Mutation 20 (3), pp. 197 - 208 (2002)
  7. 347.
    Journal Article
    Robinson, P. N.; Booms, P.; Katzke, S.; Ladewig, M.; Neumann, L. M.; Palz, M.; Pregla, R.; Tiecke, F.; Rosenberg, T.: Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies. Human Mutation 20 (3), pp. 153 - 161 (2002)
  8. 348.
    Journal Article
    Rinke-Appel, J.; Osswald, M.; von Knoblauch, K.; Mueller, F.; Brimacombe, R.; Sergiev, P.; Avdeeva, O.; Bogdanov, A.; Dontsova, O.: Crosslinking of 4.5S RNA to the Escherichia coli ribosome in the presence or absence of the protein Ffh. RNA 8 (5), pp. 612 - 625 (2002)
  9. 349.
    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)
  10. 350.
    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)
  11. 351.
    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)
  12. 352.
    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)
  13. 353.
    Journal Article
    Schultz, E. S.; Kaufmann, D.; Tinschert, S.; Schell, H.; von den Driesch, P.; Schuler, G.: Segmental Neurofibromatosis. Dermatology 204 (4), pp. 296 - 297 (2002)
  14. 354.
    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)
  15. 355.
    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)
  16. 356.
    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. 357.
    Book
    Mundlos, S.; Horn, D.: Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 pp.

Book Chapter (1)

  1. 358.
    Book Chapter
    Schulz, M. H.; Köhler, S.; Bauer, S.; Vingron, M.; Robinson, P. N.: Exact Score Distribution Computation for Similarity Searches in Ontologies. In: Algorithms in Bioinformatics, pp. 298 - 309 (Eds. Salzberg, S. L.; Warnow, T.). Springer, New York [et al] (2009)

Conference Paper (1)

  1. 359.
    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)

Talk (1)

  1. 360.
    Talk
    Ibrahim, D.; Lupiáñez, D. G.: LilBUBome - Why would you crowdfund a cute cat? Open Science Days 2016, Berlin (2016)
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