187 related articles for article (PubMed ID: 12818524)
21. Non-Invasive Prenatal Test Analysis Opens a Pandora's Box: Identification of Very Rare Cases of SRY-Positive Healthy Females, Segregating for Three Generations Thanks to Preferential Inactivation of the XqYp Translocated Chromosome.
Politi C; Grillone K; Nocera D; Colao E; Bellisario ML; Loddo S; Catino G; Novelli A; Perrotti N; Rodolfo I; Malatesta P
Genes (Basel); 2024 Jan; 15(1):. PubMed ID: 38254992
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. [The 46,XX male; a chromosomal form of a disorder of sex development].
Visser MM; Lutgers HL; van Ravenswaaij CMA
Ned Tijdschr Geneeskd; 2018 Oct; 162():. PubMed ID: 30358369
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. A del(X)(p11) carrying SRY sequences in an infant with ambiguous genitalia.
Ellaithi M; Gisselsson D; Nilsson T; Abd El-Fatah S; Ali T; Elagib A; Ibrahim ME; Fadl-Elmula I
BMC Pediatr; 2006 Apr; 6():11. PubMed ID: 16594994
[TBL] [Abstract][Full Text] [Related]
26. [Two cases of 46,XX male with chief complaint of infertility].
Yumura Y; Kanno H; Ogawa T; Saito K; Sato K; Kubota Y; Iwasaki A; Sawada T
Hinyokika Kiyo; 2003 Dec; 49(12):727-34. PubMed ID: 14978955
[TBL] [Abstract][Full Text] [Related]
27. 45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism.
Nieto K; Peña R; Palma I; Dorantes LM; Eraña L; Alvarez R; García-Cavazos R; Kofman-Alfaro S; Queipo G
Am J Med Genet A; 2004 Oct; 130A(3):311-4. PubMed ID: 15378545
[TBL] [Abstract][Full Text] [Related]
28. The first case of 38,XX (SRY-positive) disorder of sex development in a cat.
Szczerbal I; Stachowiak M; Dzimira S; Sliwa K; Switonski M
Mol Cytogenet; 2015; 8():22. PubMed ID: 25838845
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. SRY-positive 46,XX male with cryptorchidism as the only presenting clinical feature.
Moreno-García M; Sánchez Del Pozo J; Gutierrez-Díez P; Gil-Fournier B; Barreiro Miranda E
Urol Int; 2003; 71(2):219-21. PubMed ID: 12890966
[TBL] [Abstract][Full Text] [Related]
31. Functional disomy of Xp including duplication of DAX1 gene with sex reversal due to t(X;Y)(p21.2;p11.3).
Sanlaville D; Vialard F; Thépot F; Vue-Droy L; Ardalan A; Nizard P; Corré A; Devauchelle B; Martin-Denavit T; Nouchy M; Malan V; Taillemite JL; Portnoï MF
Am J Med Genet A; 2004 Jul; 128A(3):325-30. PubMed ID: 15216557
[TBL] [Abstract][Full Text] [Related]
32. Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.
Fechner PY; Rosenberg C; Stetten G; Cargile CB; Pearson PL; Smith KD; Migeon CJ; Berkovitz GD
Cytogenet Cell Genet; 1994; 66(1):22-6. PubMed ID: 8275702
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Testicular XX (SRY-Negative) Disorder of Sex Development in Cat.
De Lorenzi L; Banco B; Previderè C; Bonacina S; Romagnoli S; Grieco V; Parma P
Sex Dev; 2017; 11(4):210-216. PubMed ID: 28848109
[TBL] [Abstract][Full Text] [Related]
35. Clinical traits and molecular findings in 46,XX males.
López M; Torres L; Méndez JP; Cervantes A; Pérez-Palacios G; Erickson RP; Alfaro G; Kofman-Alfaro S
Clin Genet; 1995 Jul; 48(1):29-34. PubMed ID: 7586641
[TBL] [Abstract][Full Text] [Related]
36. 47,XXX male: A clinical and molecular study.
Ogata T; Matsuo M; Muroya K; Koyama Y; Fukutani K
Am J Med Genet; 2001 Feb; 98(4):353-6. PubMed ID: 11170081
[TBL] [Abstract][Full Text] [Related]
37. Atypical XX male with the SRY gene located at the long arm of chromosome 1 and a 1qter microdeletion.
Queralt R; Madrigal I; Vallecillos MA; Morales C; Ballescá JL; Oliva R; Soler A; Sánchez A; Margarit E
Am J Med Genet A; 2008 May; 146A(10):1335-40. PubMed ID: 18412126
[TBL] [Abstract][Full Text] [Related]
38. Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences.
Boucekkine C; Toublanc JE; Abbas N; Chaabouni S; Ouahid S; Semrouni M; Jaubert F; Toublanc M; McElreavey K; Vilain E
Clin Endocrinol (Oxf); 1994 Jun; 40(6):733-42. PubMed ID: 8033363
[TBL] [Abstract][Full Text] [Related]
39. SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite.
Margarit E; Coll MD; Oliva R; Gómez D; Soler A; Ballesta F
Am J Med Genet; 2000 Jan; 90(1):25-8. PubMed ID: 10602113
[TBL] [Abstract][Full Text] [Related]
40. [Analysis of clinical features and related genes variation in five patients with 46, XX male syndrome].
Qin XY; Dong WK; Wang W; Dong ZY; Xiao Y; Lu WL; Wang DF
Zhonghua Er Ke Za Zhi; 2016 Nov; 54(11):840-843. PubMed ID: 27806792
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
