314 related articles for article (PubMed ID: 29665107)
1. A case of a rare variant of Klinefelter syndrome, 47,XY,i(X)(q10).
Kondo T; Kuroda S; Usui K; Mori K; Asai T; Takeshima T; Kawahara T; Hamanoue H; Uemura H; Yumura Y
Andrologia; 2018 Sep; 50(7):e13024. PubMed ID: 29665107
[TBL] [Abstract][Full Text] [Related]
2. A rare case in literature: Isochromosome Xq in Klinefelter syndrome.
Simsek L; Zamani AG; Taskapu HH; Yildirim MS
Andrologia; 2019 Jun; 51(5):e13253. PubMed ID: 30746732
[TBL] [Abstract][Full Text] [Related]
3. Variant Klinefelter syndrome 47,X,i(X)(q10),Y and normal 46,XY karyotype in monozygotic adult twins.
Stemkens D; Broekmans FJ; Kastrop PM; Hochstenbach R; Smith BG; Giltay JC
Am J Med Genet A; 2007 Aug; 143A(16):1906-11. PubMed ID: 17632769
[TBL] [Abstract][Full Text] [Related]
4. Clinical, Hormonal, and Genetic Evaluation of Idiopathic Nonobstructive Azoospermia and Klinefelter Syndrome Patients.
Kim SY; Lee BY; Oh AR; Park SY; Lee HS; Seo JT
Cytogenet Genome Res; 2017; 153(4):190-197. PubMed ID: 29466784
[TBL] [Abstract][Full Text] [Related]
5. A Rare Cause of Male Infertility: 45,X/46,XY Mosaicism.
Akinsal EC; Baydilli N; Bayramov R; Ekmekcioglu O
Urol Int; 2018; 101(4):481-485. PubMed ID: 29161714
[TBL] [Abstract][Full Text] [Related]
6. Sperm retrieval from a male with the rare 47, XXYqs variant of Klinefelter syndrome for intracytoplasmic sperm injection: A case report.
Enatsu N; Enatsu Y; Okada K; Chiba K; Matsumoto Y; Kokeguchi S; Shiotani M
Andrologia; 2020 Feb; 52(1):e13489. PubMed ID: 31777105
[TBL] [Abstract][Full Text] [Related]
7. Correlation of genetic results with testicular histology, hormones and sperm retrieval in nonobstructive azoospermia patients with testis biopsy.
Liu W; Gao X; Ma G; Yan L; Chen T; Li T; Yu RM; Ma JL
Andrologia; 2017 Sep; 49(7):. PubMed ID: 27921326
[TBL] [Abstract][Full Text] [Related]
8. Mosaic status in lymphocytes of infertile men with or without Klinefelter syndrome.
Lenz P; Luetjens CM; Kamischke A; Kühnert B; Kennerknecht I; Nieschlag E
Hum Reprod; 2005 May; 20(5):1248-55. PubMed ID: 15665007
[TBL] [Abstract][Full Text] [Related]
9. Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant.
Höckner M; Pinggera GM; Günther B; Sergi C; Fauth C; Erdel M; Kotzot D
Fertil Steril; 2008 Nov; 90(5):2009.e13-7. PubMed ID: 18687426
[TBL] [Abstract][Full Text] [Related]
10. The clinical effects of isochromosome Xq in Klinefelter syndrome: report of a case and review of literature.
Demirhan O; Pazarbaşi A; Tanriverdi N; Aridoğan A; Karahan D
Genet Couns; 2009; 20(3):235-42. PubMed ID: 19852429
[TBL] [Abstract][Full Text] [Related]
11. Morphometric and cytogenetic characteristics of testicular germ cells and Sertoli cell secretory function in men with non-mosaic Klinefelter's syndrome.
Yamamoto Y; Sofikitis N; Mio Y; Loutradis D; Kaponis A; Miyagawa I
Hum Reprod; 2002 Apr; 17(4):886-96. PubMed ID: 11925377
[TBL] [Abstract][Full Text] [Related]
12. Chromosomal variants in klinefelter syndrome.
Frühmesser A; Kotzot D
Sex Dev; 2011; 5(3):109-23. PubMed ID: 21540567
[TBL] [Abstract][Full Text] [Related]
13. The feasibility of fertility preservation in adolescents with Klinefelter syndrome.
Rives N; Milazzo JP; Perdrix A; Castanet M; Joly-Hélas G; Sibert L; Bironneau A; Way A; Macé B
Hum Reprod; 2013 Jun; 28(6):1468-79. PubMed ID: 23539613
[TBL] [Abstract][Full Text] [Related]
14. Routine screening for classical azoospermia factor deletions of the Y chromosome in azoospermic patients with Klinefelter syndrome.
Choe JH; Kim JW; Lee JS; Seo JT
Asian J Androl; 2007 Nov; 9(6):815-20. PubMed ID: 17968468
[TBL] [Abstract][Full Text] [Related]
15. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
[TBL] [Abstract][Full Text] [Related]
16. [48,XXYY men with azoospermia: how to manage infertility?].
Roche C; Sonigo C; Benmiloud-Tandjaoui N; Boujenah J; Benzacken B; Poncelet C; Hugues JN
Gynecol Obstet Fertil; 2014; 42(7-8):528-32. PubMed ID: 24934769
[TBL] [Abstract][Full Text] [Related]
17. Occurrence of 47,X,i(X)(q10),Y Klinefelter variant with hypogonadotropic hypogonadism.
Sabbaghian M; Meybodi AM; Rahimian M; Sadighi Gilani MA
Fertil Steril; 2011 Aug; 96(2):e115-7. PubMed ID: 21703612
[TBL] [Abstract][Full Text] [Related]
18. A rare variant Klinefelter syndrome seen 40 years later: 47,X,del(Xq24),Y.
Özkent MS; Balasar Ö
Andrologia; 2021 Dec; 53(11):e14213. PubMed ID: 34375016
[TBL] [Abstract][Full Text] [Related]
19. What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature.
Pinti E; Lengyel A; Fekete G; Haltrich I
BMC Pediatr; 2020 Jan; 20(1):17. PubMed ID: 31931754
[TBL] [Abstract][Full Text] [Related]
20. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]