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1q21.1-Deletionssyndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "1q21.1-Deletionssyndrom" in German language version.

refsWebsite
Global rank German rank
9doi.org
2nd place
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4nih.gov
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1web.archive.org
1st place
1st place

doi.org

  • H. C. Mefford, A. J. Sharp, C. Baker u. a.: Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. In: N Engl J Med. Band 359, Nr. 16, Oktober 2008, S. 1685–1699, doi:10.1056/NEJMoa0805384, PMID 18784092, PMC 2703742 (freier Volltext).
  • H. Stefansson, D. Rujescu, S. Cichon u. a.: Large recurrent microdeletions associated with schizophrenia. In: Nature. Band 455, Nr. 7210, September 2008, S. 232–236, doi:10.1038/nature07229, PMID 18668039, PMC 2687075 (freier Volltext).
  • Jennifer L. Stone, Michael C. O Donovan u. a.: Rare chromosomal deletions and duplications increase risk of schizophrenia. In: Nature. 455, 2008, S. 237–241, doi:10.1038/nature07239.
  • M. Velinov, N. Dolzhanskaya: Clavicular pseudoarthrosis, anomalous coronary artery and extra crease of the fifth finger-previously unreported features in individuals with class II 1q21.1 microdeletions. In: Eur J Med Genet. Band 53, Nr. 4, 2010, S. 213–216, doi:10.1016/j.ejmg.2010.05.005, PMID 20573555.
  • S. J. Diskin, C. Hou, J. T. Glessner u. a.: Copy number variation at 1q21.1 associated with neuroblastoma. In: Nature. Band 459, Nr. 7249, Juni 2009, S. 987–991, doi:10.1038/nature08035, PMID 19536264, PMC 2755253 (freier Volltext).
  • Lina Basel-Vanagaite u. a.: An emerging 1q21.1 deletion-associated neurodevelopmental phenotype. In: Journal of Child Neurology. 26 (1), S. 113–116, doi:10.1177/0883073810377658
  • Douglas F. Levinson u. a.: Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications. In: Am J Psychiatry. 2011; 168, S. 302–316; doi:10.1176/appi.ajp.2010.10060876.
  • Masashi Ikeda u. a.: Copy Number Variation in Schizophrenia in the Japanese Population. In: Biological Psychiatry. Volume 67, Issue 3, S. 283–286 (1 February 2010) doi:10.1016/j.biopsych.2009.08.034.
  • Junyan Li u. a.: Common Variants in the BCL9 Gene Conferring Risk of Schizophrenia. In: Arch Gen Psychiatry. 2011;68(3), S. 232–240. doi:10.1001/archgenpsychiatry.2011.1.

nih.gov

ncbi.nlm.nih.gov

  • H. C. Mefford, A. J. Sharp, C. Baker u. a.: Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. In: N Engl J Med. Band 359, Nr. 16, Oktober 2008, S. 1685–1699, doi:10.1056/NEJMoa0805384, PMID 18784092, PMC 2703742 (freier Volltext).
  • H. Stefansson, D. Rujescu, S. Cichon u. a.: Large recurrent microdeletions associated with schizophrenia. In: Nature. Band 455, Nr. 7210, September 2008, S. 232–236, doi:10.1038/nature07229, PMID 18668039, PMC 2687075 (freier Volltext).
  • M. Velinov, N. Dolzhanskaya: Clavicular pseudoarthrosis, anomalous coronary artery and extra crease of the fifth finger-previously unreported features in individuals with class II 1q21.1 microdeletions. In: Eur J Med Genet. Band 53, Nr. 4, 2010, S. 213–216, doi:10.1016/j.ejmg.2010.05.005, PMID 20573555.
  • S. J. Diskin, C. Hou, J. T. Glessner u. a.: Copy number variation at 1q21.1 associated with neuroblastoma. In: Nature. Band 459, Nr. 7249, Juni 2009, S. 987–991, doi:10.1038/nature08035, PMID 19536264, PMC 2755253 (freier Volltext).

web.archive.org

  • Unique (Memento vom 2. September 2011 im Internet Archive), abgerufen am 11. April 2024.