45,X/46,XY mosaicism (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "45,X/46,XY mosaicism" in English language version.

refsWebsite

Global rank English rank

11nih.gov

4^th place

6doi.org

2^nd place

2web.archive.org

1^st place

1rarechromo.org

low place

1semanticscholar.org

11^th place

8^th place

1orpha.net

3,537^th place

7,177^th place

1aappublications.org

3,763^rd place

3,602^nd place

aappublications.org

pediatrics.aappublications.org

45,X/46,XY Mosaicism: Report of 27 Cases Archived 2019-12-16 at the Wayback Machine. Pediatrics Vol. 104 No. 2 August 1, 1999. pp. 304 -308

doi.org

Johansen, Marie Lindhart; et al. (1 August 2012). "45,X/46,XY Mosaicism: Phenotypic Characteristics, Growth, and Reproductive Function—A Retrospective Longitudinal Study". The Journal of Clinical Endocrinology & Metabolism. 97 (8): E1540 – E1549. doi:10.1210/jc.2012-1388. PMID 22605431.
Zhou W, Machiela MJ, Freedman ND, Rothman N, Malats N, Dagnall C, et al. (2016). "Mosaic loss of chromosome Y is associated with common variation near TCL1A". Nat Genet. 48 (5): 563–8. doi:10.1038/ng.3545. PMC 4848121. PMID 27064253.
Kim KR, Kwon Y, Joung JY, Kim KS, Ayala AG, Ro JY (October 2002). "True hermaphroditism and mixed gonadal dysgenesis in young children: a clinicopathologic study of 10 cases". Mod. Pathol. 15 (10): 1013–9. doi:10.1097/01.MP.0000027623.23885.0D. PMID 12379746.
Hsu LY (January 1989). "Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update". Prenat. Diagn. 9 (1): 31–48. doi:10.1002/pd.1970090106. PMID 2664755. S2CID 20193032.
Efthymiadou A, Stefanou EG, Chrysis D (2012). "45,X/46,XY mosaicism: a cause of short stature in males". Hormones (Athens). 11 (4): 501–4. doi:10.14310/horm.2002.1384. PMID 23422775.
Donahoe PK, Crawford JD, Hendren WH (1979). "Mixed gonadal dysgenesis, pathogenesis, and management". J. Pediatr. Surg. 14 (3): 287–300. doi:10.1016/S0022-3468(79)80486-8. PMID 480090.

nih.gov

pubmed.ncbi.nlm.nih.gov

Johansen, Marie Lindhart; et al. (1 August 2012). "45,X/46,XY Mosaicism: Phenotypic Characteristics, Growth, and Reproductive Function—A Retrospective Longitudinal Study". The Journal of Clinical Endocrinology & Metabolism. 97 (8): E1540 – E1549. doi:10.1210/jc.2012-1388. PMID 22605431.
Zhou W, Machiela MJ, Freedman ND, Rothman N, Malats N, Dagnall C, et al. (2016). "Mosaic loss of chromosome Y is associated with common variation near TCL1A". Nat Genet. 48 (5): 563–8. doi:10.1038/ng.3545. PMC 4848121. PMID 27064253.
Chang, H. J.; Clark, R. D.; Bachman, H. (1990). "The phenotype of 45,X/46,XY mosaicism: An analysis of 92 prenatally diagnosed cases". American Journal of Human Genetics. 46 (1): 156–167. PMC 1683543. PMID 2294747.
Kim KR, Kwon Y, Joung JY, Kim KS, Ayala AG, Ro JY (October 2002). "True hermaphroditism and mixed gonadal dysgenesis in young children: a clinicopathologic study of 10 cases". Mod. Pathol. 15 (10): 1013–9. doi:10.1097/01.MP.0000027623.23885.0D. PMID 12379746.
Hsu LY (January 1989). "Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update". Prenat. Diagn. 9 (1): 31–48. doi:10.1002/pd.1970090106. PMID 2664755. S2CID 20193032.
Chang, H J; et al. (1990). "The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases". American Journal of Human Genetics. 46 (1): 156–167. PMC 1683543. PMID 2294747.
Efthymiadou A, Stefanou EG, Chrysis D (2012). "45,X/46,XY mosaicism: a cause of short stature in males". Hormones (Athens). 11 (4): 501–4. doi:10.14310/horm.2002.1384. PMID 23422775.
Donahoe PK, Crawford JD, Hendren WH (1979). "Mixed gonadal dysgenesis, pathogenesis, and management". J. Pediatr. Surg. 14 (3): 287–300. doi:10.1016/S0022-3468(79)80486-8. PMID 480090.

ncbi.nlm.nih.gov

Zhou W, Machiela MJ, Freedman ND, Rothman N, Malats N, Dagnall C, et al. (2016). "Mosaic loss of chromosome Y is associated with common variation near TCL1A". Nat Genet. 48 (5): 563–8. doi:10.1038/ng.3545. PMC 4848121. PMID 27064253.
Chang, H. J.; Clark, R. D.; Bachman, H. (1990). "The phenotype of 45,X/46,XY mosaicism: An analysis of 92 prenatally diagnosed cases". American Journal of Human Genetics. 46 (1): 156–167. PMC 1683543. PMID 2294747.
Chang, H J; et al. (1990). "The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases". American Journal of Human Genetics. 46 (1): 156–167. PMC 1683543. PMID 2294747.

orpha.net

45,X/46,XY mixed gonadal dysgenesis Archived 2017-04-17 at the Wayback Machine. Orfa.net; August 2015.

rarechromo.org

"45,X/46,XY including Y chromosome rearrangements" (PDF). rarechromo.org. Retrieved 15 July 2024.

semanticscholar.org

api.semanticscholar.org

Hsu LY (January 1989). "Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update". Prenat. Diagn. 9 (1): 31–48. doi:10.1002/pd.1970090106. PMID 2664755. S2CID 20193032.

web.archive.org

45,X/46,XY mixed gonadal dysgenesis Archived 2017-04-17 at the Wayback Machine. Orfa.net; August 2015.
45,X/46,XY Mosaicism: Report of 27 Cases Archived 2019-12-16 at the Wayback Machine. Pediatrics Vol. 104 No. 2 August 1, 1999. pp. 304 -308