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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1970 | 1 |
1976 | 1 |
1987 | 1 |
2012 | 1 |
2013 | 2 |
2021 | 1 |
2023 | 1 |
2024 | 0 |
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Page 1
Cytogenic and molecular analyses of 46,XX male syndrome with clinical comparison to other groups with testicular azoospermia of genetic origin.
J Formos Med Assoc. 2013 Feb;112(2):72-8. doi: 10.1016/j.jfma.2012.02.009. Epub 2012 Aug 30.
J Formos Med Assoc. 2013.
PMID: 23380608
Free article.
Clinical, cytogenetic, and molecular analysis with 46,XX male sex reversal syndrome: case reports.
Gao X, Chen G, Huang J, Bai Q, Zhao N, Shao M, Jiao L, Wei Y, Chang L, Li D, Yang L.
Gao X, et al.
J Assist Reprod Genet. 2013 Mar;30(3):431-5. doi: 10.1007/s10815-013-9939-7. Epub 2013 Feb 3.
J Assist Reprod Genet. 2013.
PMID: 23378127
Free PMC article.
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Ventral-Onlay Buccal Mucosal Graft Urethroplasty of a Perineal Fistula in a 26-Year-Old Patient With 46 XX Male Syndrome: A Case Report.
Hosseini J, Zamani Hajiabadi A, Mirjalili AM.
Hosseini J, et al.
Am J Mens Health. 2023 Mar-Apr;17(2):15579883231156663. doi: 10.1177/15579883231156663.
Am J Mens Health. 2023.
PMID: 37038331
Free PMC article.
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A case of XX male syndrome.
Lisker R, Flores F, Cobo A, Rojas FG.
Lisker R, et al.
J Med Genet. 1970 Dec;7(4):394-8. doi: 10.1136/jmg.7.4.394.
J Med Genet. 1970.
PMID: 5501706
Free PMC article.
No abstract available.
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[Male infertility with chromosomal abnormalities. II. XX-male syndrome].
Hazama M, Kondo K, Fujisawa M, Maeda H, Okamoto Y, Oka N, Ren KZ, Hamaguchi T, Yamazaki H, Okada H, et al.
Hazama M, et al.
Hinyokika Kiyo. 1987 Feb;33(2):193-203.
Hinyokika Kiyo. 1987.
PMID: 3591582
Free article.
Japanese.
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Generation of a human induced pluripotent stem cell line (SMUSHi001-A) from a patient with 46, XX male sex reversal syndrome carrying the SRY gene.
Yan R, Wu S, Wang W, Chu M, Liu P.
Yan R, et al.
Stem Cell Res. 2021 Jul;54:102397. doi: 10.1016/j.scr.2021.102397. Epub 2021 May 24.
Stem Cell Res. 2021.
PMID: 34098200
Free article.
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A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).
Ventruto V, Cali A, Farina L, Festa B, Ricciardi I, Sebastio L.
Ventruto V, et al.
J Med Genet. 1976 Feb;13(1):71-5. doi: 10.1136/jmg.13.1.71.
J Med Genet. 1976.
PMID: 1271431
Free PMC article.
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