172 related articles for article (PubMed ID: 18412126)
21. Localization of the sex-determining region-Y gene in XX males.
Suzuki Y; Sasagawa I; Yazawa H; Tateno T; Nakada T; Saito H; Hiroi M
Arch Androl; 2000; 44(2):133-6. PubMed ID: 10746870
[TBL] [Abstract][Full Text] [Related]
22. 46,XX males: a case series based on clinical and genetics evaluation.
Mohammadpour Lashkari F; Totonchi M; Zamanian MR; Mansouri Z; Sadighi Gilani MA; Sabbaghian M; Mohseni Meybodi A
Andrologia; 2017 Sep; 49(7):. PubMed ID: 27882599
[TBL] [Abstract][Full Text] [Related]
23. Analysis of SRY gene in 8 cases of sex abnormality.
Wang H; Teng Y; Tian H; Tang Y; Chen Y; Yang Z
J Huazhong Univ Sci Technolog Med Sci; 2004; 24(5):503-6. PubMed ID: 15641705
[TBL] [Abstract][Full Text] [Related]
24. Delineation of the cryptic 1qter deletion phenotype.
Merritt JL; Zou Y; Jalal SM; Michels VV
Am J Med Genet A; 2007 Mar; 143A(6):599-603. PubMed ID: 17304549
[TBL] [Abstract][Full Text] [Related]
25. An infertile 45,X male with a SRY-bearing chromosome 13: a clinical case report and literature review.
Peng D; Zhang YS; Zhang XY; Hu C; Liu MH; Liu RZ
J Assist Reprod Genet; 2015 Jan; 32(1):107-9. PubMed ID: 25374395
[TBL] [Abstract][Full Text] [Related]
26. Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome.
Poplinski A; Wieacker P; Kliesch S; Gromoll J
Eur J Endocrinol; 2010 Jan; 162(1):169-75. PubMed ID: 19812237
[TBL] [Abstract][Full Text] [Related]
27. Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report.
Pinho MJ; Neves R; Costa P; Ferrás C; Sousa M; Alves C; Almeida C; Fernandes S; Silva J; Ferrás L; Barros A
Hum Reprod; 2005 Mar; 20(3):689-96. PubMed ID: 15665019
[TBL] [Abstract][Full Text] [Related]
28. Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.
Castro A; Rodríguez F; Flórez M; López P; Curotto B; Martínez D; Maturana A; Lardone MC; Palma C; Mericq V; Ebensperger M; Cassorla F
Hum Reprod; 2017 Feb; 32(2):465-475. PubMed ID: 28057878
[TBL] [Abstract][Full Text] [Related]
29. Localization of SRY by primed in situ labeling in XX and XY sex reversal.
Kadandale JS; Wachtel SS; Tunca Y; Wilroy RS; Martens PR; Tharapel AT
Am J Med Genet; 2000 Nov; 95(1):71-4. PubMed ID: 11074498
[TBL] [Abstract][Full Text] [Related]
30. SRY-negative 46,XX infertile male with Leydig cell hyperplasia: clinical, cytogenetic, and molecular analysis and review of the literature.
Kim JW; Bak CW; Chin MU; Cha DH; Yoon TK; Shim SH
Fertil Steril; 2010 Jul; 94(2):753.e5-9. PubMed ID: 20227075
[TBL] [Abstract][Full Text] [Related]
31. Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe.
Magenis RE; Casanova M; Fellous M; Olson S; Sheehy R
Hum Genet; 1987 Mar; 75(3):228-33. PubMed ID: 3557449
[TBL] [Abstract][Full Text] [Related]
32. Male patient 46,XX SRY-negative and unambiguous genitalia: A case report.
Casas-Vargas A; Galvis J; Blanco J; Rengifo L; Usaquén W; Velasco H
Biomedica; 2019 Dec; 39(4):622-630. PubMed ID: 31860174
[TBL] [Abstract][Full Text] [Related]
33. An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12).
Wu J; Hu G; Zhai J; Han C; Li Z
Clin Case Rep; 2022 Jul; 10(7):e5984. PubMed ID: 35846903
[TBL] [Abstract][Full Text] [Related]
34. An Infertile Azoospermic Male With 45, X T(Yp;15) Karyotype.
Abiri M; Hassanlou M; Narimani N; Zamani M; Moeini Z
J Family Reprod Health; 2021 Dec; 15(4):271-274. PubMed ID: 35340802
[No Abstract] [Full Text] [Related]
35. Infertility in a new 46, XX male with positive SRY confirmed by fluorescence in situ hybridization: a case report.
Pepene CE; Coman I; Mihu D; Militaru M; Duncea I
Clin Exp Obstet Gynecol; 2008; 35(4):299-300. PubMed ID: 19205451
[TBL] [Abstract][Full Text] [Related]
36. Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY.
Van der Auwera B; Van Roy N; De Paepe A; Hawkins JR; Liebaers I; Castedo S; Dumon J; Speleman F
Hum Genet; 1992 Apr; 89(1):23-8. PubMed ID: 1577463
[TBL] [Abstract][Full Text] [Related]
37. Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.
Margarit E; Soler A; Carrió A; Oliva R; Costa D; Vendrell T; Rosell J; Ballesta F
J Med Genet; 1998 Sep; 35(9):727-30. PubMed ID: 9733030
[TBL] [Abstract][Full Text] [Related]
38. A case report of an incidental finding of a 46,XX, SRY-negative male with masculine phenotype during standard fertility workup with review of the literature and proposed immediate and long-term management guidance.
Ryan NA; Akbar S
Fertil Steril; 2013 Apr; 99(5):1273-6. PubMed ID: 23290744
[TBL] [Abstract][Full Text] [Related]
39. [Genotypic sex and phenotypic sex: clinical, biochemical and molecular aspects in a patient with male hypogonadism and 46XX-45XO karyotype].
Torre R; Savino A; Venturi P; Taverna R; Triacca R; Coli A; Bernasconi D; Del Monte P; Marugo M
Recenti Prog Med; 2001 Dec; 92(12):747-50. PubMed ID: 11822095
[TBL] [Abstract][Full Text] [Related]
40. Karyotype analysis in large sample cases from Shenyang Women's and Children's hospital: a study of 16,294 male infertility patients.
Gao M; Pang H; Zhao YH; Hua J; Tong D; Zhao H; Liu Y; Zhao Y; Zhang M; Yan XJ; Chen H; Ma HP; Jin TY; Dong SL
Andrologia; 2017 May; 49(4):. PubMed ID: 27397756
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]