XXYY syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "XXYY syndrome" in English language version.

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Tartaglia N, Davis S, Hench A, et al. (June 2008). "A New Look at XXYY Syndrome: Medical and Psychological Features". American Journal of Medical Genetics Part A. 146A (12): 1509–22. doi:10.1002/ajmg.a.32366. PMC 3056496. PMID 18481271.
Visootsak J, Rosner B, Dykens E, Tartaglia N, Graham JM, Jr (2007). "Behavioral phenotype of sex chromosome aneuploidies: 48, XXYY, 48, XXXY, and 49,XXXXY". American Journal of Medical Genetics Part A. 143A (11): 1198–1203. doi:10.1002/ajmg.a.31746. PMID 17497714. S2CID 25732790.
Muldal S, Ockey CH (August 27, 1960). "The "double male": a new chromosome constitution in Klinefelter's syndrome". Lancet. 276 (7147): 492–3. doi:10.1016/S0140-6736(60)91624-X.

"48,XXYY syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 13 January 2020. Retrieved 19 May 2019.
"48,XXYY syndrome". Genetics and Rare Diseases Information Center. Retrieved 20 February 2023.
"48,XXYY syndrome". Genetics and Rare Diseases Information Center. NIH.

Tartaglia N, Davis S, Hench A, et al. (June 2008). "A New Look at XXYY Syndrome: Medical and Psychological Features". American Journal of Medical Genetics Part A. 146A (12): 1509–22. doi:10.1002/ajmg.a.32366. PMC 3056496. PMID 18481271.
Visootsak J, Rosner B, Dykens E, Tartaglia N, Graham JM, Jr (2007). "Behavioral phenotype of sex chromosome aneuploidies: 48, XXYY, 48, XXXY, and 49,XXXXY". American Journal of Medical Genetics Part A. 143A (11): 1198–1203. doi:10.1002/ajmg.a.31746. PMID 17497714. S2CID 25732790.

Tartaglia N, Davis S, Hench A, et al. (June 2008). "A New Look at XXYY Syndrome: Medical and Psychological Features". American Journal of Medical Genetics Part A. 146A (12): 1509–22. doi:10.1002/ajmg.a.32366. PMC 3056496. PMID 18481271.

Visootsak J, Rosner B, Dykens E, Tartaglia N, Graham JM, Jr (2007). "Behavioral phenotype of sex chromosome aneuploidies: 48, XXYY, 48, XXXY, and 49,XXXXY". American Journal of Medical Genetics Part A. 143A (11): 1198–1203. doi:10.1002/ajmg.a.31746. PMID 17497714. S2CID 25732790.

Brown, Phyllis (2007). "Researchers define characteristics, treatment options for XXYY Syndrome". University of California. Archived from the original on April 1, 2010. Retrieved November 6, 2009.

"48,XXYY syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 13 January 2020. Retrieved 19 May 2019.
Brown, Phyllis (2007). "Researchers define characteristics, treatment options for XXYY Syndrome". University of California. Archived from the original on April 1, 2010. Retrieved November 6, 2009.