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シンプソン・ゴラビ・ベーメル症候群 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "シンプソン・ゴラビ・ベーメル症候群" in Japanese language version.

refsWebsite
Global rank Japanese rank
12nih.gov
4th place
24th place
9doi.org
2nd place
6th place
1omim.org
4,380th place
low place
1worldcat.org
5th place
19th place
1shouman.jp
low place
low place

doi.org

  • Garganta, C. L.; Bodurtha, J. N. (1992-09-15). “Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature”. American Journal of Medical Genetics 44 (2): 129–135. doi:10.1002/ajmg.1320440202. ISSN 0148-7299. PMID 1456279. https://pubmed.ncbi.nlm.nih.gov/1456279. 
  • Lapunzina, Pablo (15 August 2005). “Risk of tumorigenesis in overgrowth syndromes: A comprehensive review”. American Journal of Medical Genetics Part C 137C (1): 53–71. doi:10.1002/ajmg.c.30064. PMID 16010678. 
  • Slavotinek, Anne M. (15 May 2007). “Single gene disorders associated with congenital diaphragmatic hernia”. American Journal of Medical Genetics Part C 145C (2): 172–183. doi:10.1002/ajmg.c.30125. PMID 17436300. 
  • Slavotinek, Anne M. (15 May 2007). “Single gene disorders associated with congenital diaphragmatic hernia”. American Journal of Medical Genetics Part C 145C (2): 172–183. doi:10.1002/ajmg.c.30125. PMID 17436300. 
  • Chen, Chih-Ping (1 June 2012). “Prenatal findings and the genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome”. Taiwanese Journal of Obstetrics and Gynecology 51 (2): 186–191. doi:10.1016/j.tjog.2012.04.004. PMID 22795092. 
  • Veugelers, M.4; Cat, BD; Muyldermans, SY; Reekmans, G; Delande, N; Frints, S; Legius, E; Fryns, JP et al. (22 May 2000). “Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene”. Human Molecular Genetics 9 (9): 1321–1328. doi:10.1093/hmg/9.9.1321. PMID 10814714. 
  • Vora, Neeta; Bianchi, Diana W. (1 October 2009). “Genetic considerations in the prenatal diagnosis of overgrowth syndromes”. Prenatal Diagnosis 29 (10): 923–929. doi:10.1002/pd.2319. PMC 4426974. PMID 19609940. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426974/. 
  • DeBaun, Michael R.; Ess, Jennifer; Saunders, Scott (1 April 2001). “Simpson Golabi Behmel Syndrome: Progress toward Understanding the Molecular Basis for Overgrowth, Malformation, and Cancer Predisposition”. Molecular Genetics and Metabolism 72 (4): 279–286. doi:10.1006/mgme.2001.3150. PMID 11286501. 
  • Wabitsch, Martin (January 2001). “Characterization of a human preadipocyte cell strain with high capacity for adipose differentiation”. International Journal of Obesity and Related Metabolic Disorders 25 (1): 8–15. doi:10.1038/sj.ijo.0801520. PMID 11244452. 

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Garganta, C. L.; Bodurtha, J. N. (1992-09-15). “Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature”. American Journal of Medical Genetics 44 (2): 129–135. doi:10.1002/ajmg.1320440202. ISSN 0148-7299. PMID 1456279. https://pubmed.ncbi.nlm.nih.gov/1456279. 
  • Lapunzina, Pablo (15 August 2005). “Risk of tumorigenesis in overgrowth syndromes: A comprehensive review”. American Journal of Medical Genetics Part C 137C (1): 53–71. doi:10.1002/ajmg.c.30064. PMID 16010678. 
  • Slavotinek, Anne M. (15 May 2007). “Single gene disorders associated with congenital diaphragmatic hernia”. American Journal of Medical Genetics Part C 145C (2): 172–183. doi:10.1002/ajmg.c.30125. PMID 17436300. 
  • Slavotinek, Anne M. (15 May 2007). “Single gene disorders associated with congenital diaphragmatic hernia”. American Journal of Medical Genetics Part C 145C (2): 172–183. doi:10.1002/ajmg.c.30125. PMID 17436300. 
  • Chen, Chih-Ping (1 June 2012). “Prenatal findings and the genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome”. Taiwanese Journal of Obstetrics and Gynecology 51 (2): 186–191. doi:10.1016/j.tjog.2012.04.004. PMID 22795092. 
  • Veugelers, M.4; Cat, BD; Muyldermans, SY; Reekmans, G; Delande, N; Frints, S; Legius, E; Fryns, JP et al. (22 May 2000). “Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene”. Human Molecular Genetics 9 (9): 1321–1328. doi:10.1093/hmg/9.9.1321. PMID 10814714. 
  • Vora, Neeta; Bianchi, Diana W. (1 October 2009). “Genetic considerations in the prenatal diagnosis of overgrowth syndromes”. Prenatal Diagnosis 29 (10): 923–929. doi:10.1002/pd.2319. PMC 4426974. PMID 19609940. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426974/. 
  • DeBaun, Michael R.; Ess, Jennifer; Saunders, Scott (1 April 2001). “Simpson Golabi Behmel Syndrome: Progress toward Understanding the Molecular Basis for Overgrowth, Malformation, and Cancer Predisposition”. Molecular Genetics and Metabolism 72 (4): 279–286. doi:10.1006/mgme.2001.3150. PMID 11286501. 
  • Wabitsch, Martin (January 2001). “Characterization of a human preadipocyte cell strain with high capacity for adipose differentiation”. International Journal of Obesity and Related Metabolic Disorders 25 (1): 8–15. doi:10.1038/sj.ijo.0801520. PMID 11244452. 

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

omim.org

shouman.jp

worldcat.org

search.worldcat.org

  • Garganta, C. L.; Bodurtha, J. N. (1992-09-15). “Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature”. American Journal of Medical Genetics 44 (2): 129–135. doi:10.1002/ajmg.1320440202. ISSN 0148-7299. PMID 1456279. https://pubmed.ncbi.nlm.nih.gov/1456279.