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WAGR-Syndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "WAGR-Syndrom" in German language version.

refsWebsite
Global rank German rank
8doi.org
2nd place
3rd place
8nih.gov
4th place
7th place
1omim.org
4,380th place
781st place

doi.org

  • B. V. Fischbach, K. L. Trout, J. Lewis, C. A. Luis, M. Sika: WAGR syndrome: a clinical review of 54 cases. In: Pediatrics. Band 116, Nr. 4, 2005, S. 984–988, doi:10.1542/peds.2004-0467, PMID 16199712.
  • C. Turleau, J. de Grouchy, C. Nihoul-Fékété, J. Dufier, F. Chavin-Colin, C. Junien: Del11p13/nephroblastoma without aniridia. In: Hum Genet. Band 67, Nr. 4, 1984, S. 455–456, doi:10.1007/BF00291410, PMID 6092262.
  • T. Glaser, L. Jepeal, J. Edwards, S. Young, J. Favor, R. Maas: PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. In: Nat Genet. Band 7, Nr. 4, 1994, S. 463–471, doi:10.1038/ng0894-463, PMID 7951315.
  • T. Yasuda, Y. Kajimoto, Y. Fujitani, H. Watada, S. Yamamoto, T. Watarai, Y. Umayahara, M. Matsuhisa, S. Gorogawa, Y. Kuwayama, Y. Tano, Y. Yamasaki, M. Hori: PAX6 mutation as a genetic factor common to aniridia and glucose intolerance. In: Diabetes. Band 51, Nr. 1, 2002, S. 224–230, doi:10.2337/diabetes.51.1.224, PMID 11756345.
  • T. Mitchell, S. Free, K. Williamson, J. Stevens, A. Churchill, I. Hanson, S. Shorvon, A. Moore, V. van Heyningen, S. Sisodiya: Polymicrogyria and absence of pineal gland due to PAX6 mutation. In: Ann Neurol. Band 53, Nr. 5, 2003, S. 658–663, doi:10.1002/ana.10576, PMID 12731001.
  • A. Talamillo, J. Quinn, J. Collinson, D. Caric, D. Price, J. West, R. Hill: Pax6 regulates regional development and neuronal migration in the cerebral cortex. In: Dev Biol. Band 255, Nr. 1, 2003, S. 151–163, doi:10.1016/S0012-1606(02)00046-5, PMID 12618140.
  • J. C. Han, Q. R. Liu, M. Jones u. a.: Brain-derived neurotrophic factor and obesity in the WAGR syndrome. In: N. Engl. J. Med. Band 359, Nr. 9, August 2008, S. 918–927, doi:10.1056/NEJMoa0801119, PMID 18753648, PMC 2553704 (freier Volltext).
  • Robert W. Miller, Joseph F. Fraumeni, Miriam D. Manning: Association of Wilms's tumour with aniridia, hemihypertrophy and other congenital malformations. In: N Engl J Med. Band 270, Nr. 18, 1964, S. 922–927, doi:10.1056/NEJM196404302701802, PMID 14114111.

nih.gov

ncbi.nlm.nih.gov

  • B. V. Fischbach, K. L. Trout, J. Lewis, C. A. Luis, M. Sika: WAGR syndrome: a clinical review of 54 cases. In: Pediatrics. Band 116, Nr. 4, 2005, S. 984–988, doi:10.1542/peds.2004-0467, PMID 16199712.
  • C. Turleau, J. de Grouchy, C. Nihoul-Fékété, J. Dufier, F. Chavin-Colin, C. Junien: Del11p13/nephroblastoma without aniridia. In: Hum Genet. Band 67, Nr. 4, 1984, S. 455–456, doi:10.1007/BF00291410, PMID 6092262.
  • T. Glaser, L. Jepeal, J. Edwards, S. Young, J. Favor, R. Maas: PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. In: Nat Genet. Band 7, Nr. 4, 1994, S. 463–471, doi:10.1038/ng0894-463, PMID 7951315.
  • T. Yasuda, Y. Kajimoto, Y. Fujitani, H. Watada, S. Yamamoto, T. Watarai, Y. Umayahara, M. Matsuhisa, S. Gorogawa, Y. Kuwayama, Y. Tano, Y. Yamasaki, M. Hori: PAX6 mutation as a genetic factor common to aniridia and glucose intolerance. In: Diabetes. Band 51, Nr. 1, 2002, S. 224–230, doi:10.2337/diabetes.51.1.224, PMID 11756345.
  • T. Mitchell, S. Free, K. Williamson, J. Stevens, A. Churchill, I. Hanson, S. Shorvon, A. Moore, V. van Heyningen, S. Sisodiya: Polymicrogyria and absence of pineal gland due to PAX6 mutation. In: Ann Neurol. Band 53, Nr. 5, 2003, S. 658–663, doi:10.1002/ana.10576, PMID 12731001.
  • A. Talamillo, J. Quinn, J. Collinson, D. Caric, D. Price, J. West, R. Hill: Pax6 regulates regional development and neuronal migration in the cerebral cortex. In: Dev Biol. Band 255, Nr. 1, 2003, S. 151–163, doi:10.1016/S0012-1606(02)00046-5, PMID 12618140.
  • J. C. Han, Q. R. Liu, M. Jones u. a.: Brain-derived neurotrophic factor and obesity in the WAGR syndrome. In: N. Engl. J. Med. Band 359, Nr. 9, August 2008, S. 918–927, doi:10.1056/NEJMoa0801119, PMID 18753648, PMC 2553704 (freier Volltext).
  • Robert W. Miller, Joseph F. Fraumeni, Miriam D. Manning: Association of Wilms's tumour with aniridia, hemihypertrophy and other congenital malformations. In: N Engl J Med. Band 270, Nr. 18, 1964, S. 922–927, doi:10.1056/NEJM196404302701802, PMID 14114111.

omim.org