Trippel-X (Swedish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Trippel-X" in Swedish language version.

refsWebsite

Global rank Swedish rank

4^th place

17^th place

5^th place

9^th place

1lakartidningen.se

low place

148^th place

2^nd place

14^th place

doi.org

dx.doi.org

Otter, Maarten; Schrander-Stumpel, Constance T. R. M.; Curfs, Leopold M. G.. ”Triple X syndrome: a review of the literature”. European journal of human genetics: EJHG 18 (3): sid. 265–271. doi:10.1038/ejhg.2009.109. ISSN 1476-5438. https://www.ncbi.nlm.nih.gov/pubmed/19568271. Läst 9 juli 2017.

lakartidningen.se

Gustavsson, Karl-Henrik (1999). ”Trippel-X – kromosomavvikelse med lindriga symtom”. Läkartidningen 96 (50): sid. 5646. https://lakartidningen.se/wp-content/uploads/OldPdfFiles/1999/20410.pdf.

nih.gov

ncbi.nlm.nih.gov

Li, Mingyan; Zou, Chaochun; Zhao, Zhengyan (2012-6). ”Triple X Syndrome with Short Stature: Case Report and Literature Review”. Iranian Journal of Pediatrics 22 (2): sid. 269–273. ISSN 2008-2142. PMID 23056899. PMC: 3446055. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446055/. Läst 26 oktober 2019.
Otter, Maarten; Schrander-Stumpel, Constance T. R. M.; Curfs, Leopold M. G.. ”Triple X syndrome: a review of the literature”. European journal of human genetics: EJHG 18 (3): sid. 265–271. doi:10.1038/ejhg.2009.109. ISSN 1476-5438. https://www.ncbi.nlm.nih.gov/pubmed/19568271. Läst 9 juli 2017.

ghr.nlm.nih.gov

Reference, Genetics Home. ”Triple X syndrome” (på engelska). Genetics Home Reference. https://ghr.nlm.nih.gov/condition/triple-x-syndrome. Läst 26 oktober 2019.

worldcat.org

Li, Mingyan; Zou, Chaochun; Zhao, Zhengyan (2012-6). ”Triple X Syndrome with Short Stature: Case Report and Literature Review”. Iranian Journal of Pediatrics 22 (2): sid. 269–273. ISSN 2008-2142. PMID 23056899. PMC: 3446055. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446055/. Läst 26 oktober 2019.
Otter, Maarten; Schrander-Stumpel, Constance T. R. M.; Curfs, Leopold M. G.. ”Triple X syndrome: a review of the literature”. European journal of human genetics: EJHG 18 (3): sid. 265–271. doi:10.1038/ejhg.2009.109. ISSN 1476-5438. https://www.ncbi.nlm.nih.gov/pubmed/19568271. Läst 9 juli 2017.