183 related articles for article (PubMed ID: 10680293)
1. A study of 45,X/46,XX mosaicism in Turner syndrome females: a novel primer pair for the (CAG)n repeat within the androgen receptor gene.
Leonova J; Hanson C
Hereditas; 1999; 131(2):87-92. PubMed ID: 10680293
[TBL] [Abstract][Full Text] [Related]
2. Size of the exon 1-CAG repeats of the androgen receptor gene employed as a molecular marker in the diagnosis of Turner syndrome in girls with short stature.
Figueiredo CC; Kochi C; Longui CA; Rocha MN; Richeti F; Evangelista NM; Calliari LE; Monte O
Genet Mol Res; 2008 Jan; 7(1):43-9. PubMed ID: 18273818
[TBL] [Abstract][Full Text] [Related]
3. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome.
Araújo A; Ramos ES
Braz J Med Biol Res; 2008 May; 41(5):368-72. PubMed ID: 18545811
[TBL] [Abstract][Full Text] [Related]
4. X chromosome inactivation patterns in 45,X/46,XX mosaics.
Uehara S; Sato K; Hashiyada M; Obara Y; Matsuzaki S; Nata M; Okamura K
J Hum Genet; 2001; 46(3):126-31. PubMed ID: 11310579
[TBL] [Abstract][Full Text] [Related]
5. PCR-based detection of mosaicism in Turner syndrome patients.
Yorifuji T; Muroi J; Kawai M; Sasaki H; Momoi T; Furusho K
Hum Genet; 1997 Jan; 99(1):62-5. PubMed ID: 9003496
[TBL] [Abstract][Full Text] [Related]
6. A unique mosaic Turner syndrome patient with androgen receptor gene derived marker chromosome.
Kalkan R; Özdağ N; Bundak R; Çirakoğlu A; Serakinci N
Syst Biol Reprod Med; 2016; 62(1):77-83. PubMed ID: 26744914
[TBL] [Abstract][Full Text] [Related]
7. Turner syndrome: a study of chromosomal mosaicism.
Fernández R; Méndez J; Pásaro E
Hum Genet; 1996 Jul; 98(1):29-35. PubMed ID: 8682502
[TBL] [Abstract][Full Text] [Related]
8. Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes.
Yorifuji T; Muroi J; Kawai M; Uematsu A; Sasaki H; Momoi T; Kaji M; Yamanaka C; Furusho K
J Med Genet; 1998 Jul; 35(7):539-44. PubMed ID: 9678697
[TBL] [Abstract][Full Text] [Related]
9. Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetus.
Harada N; Abe K; Nishimura T; Sasaki K; Ishikawa M; Fujimoto M; Matsumoto T; Niikawa N
Am J Med Genet; 1998 Feb; 75(4):432-7. PubMed ID: 9482654
[TBL] [Abstract][Full Text] [Related]
10. Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism.
Lorda-Sanchez I; Trujillo MJ; Gomez-Garre P; de Alba MR; Gonzalez-Gonzalez C; García-Hoyos M; Ayuso C; Ramos C
Am J Med Genet A; 2003 Aug; 121A(1):20-4. PubMed ID: 12900896
[TBL] [Abstract][Full Text] [Related]
11. Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?
Held KR; Kerber S; Kaminsky E; Singh S; Goetz P; Seemanova E; Goedde HW
Hum Genet; 1992 Jan; 88(3):288-94. PubMed ID: 1733830
[TBL] [Abstract][Full Text] [Related]
12. A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX.
Gray BA; Bent-Williams A; Wolff DJ; Zori RT
Clin Genet; 2001 Jul; 60(1):73-6. PubMed ID: 11531974
[TBL] [Abstract][Full Text] [Related]
13. Molecular detection of XO - Turner syndrome.
Longui CA; Rocha MN; Martinho LC; Gomes GG; de Miranda RE; Lima TA; Melo MB; Monte O
Genet Mol Res; 2002 Sep; 1(3):266-70. PubMed ID: 14963834
[TBL] [Abstract][Full Text] [Related]
14. Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype.
Uematsu A; Yorifuji T; Muroi J; Kawai M; Mamada M; Kaji M; Yamanaka C; Momoi T; Nakahata T
Am J Med Genet; 2002 Aug; 111(2):134-9. PubMed ID: 12210339
[TBL] [Abstract][Full Text] [Related]
15. Parental origin of the X chromosome, X chromosome mosaicism and screening for "hidden" Y chromosome in 45,X Turner syndrome ascertained cytogenetically.
Larsen T; Gravholt CH; Tillebeck A; Larsen H; Jensen MB; Nielsen J; Friedrich U
Clin Genet; 1995 Jul; 48(1):6-11. PubMed ID: 7586647
[TBL] [Abstract][Full Text] [Related]
16. Analysis of sex chromosome aneuploidy in 41 patients with Turner syndrome: a study of 'hidden' mosaicism.
Fernández-García R; García-Doval S; Costoya S; Pásaro E
Clin Genet; 2000 Sep; 58(3):201-8. PubMed ID: 11076042
[TBL] [Abstract][Full Text] [Related]
17. Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability.
La Spada AR; Peterson KR; Meadows SA; McClain ME; Jeng G; Chmelar RS; Haugen HA; Chen K; Singer MJ; Moore D; Trask BJ; Fischbeck KH; Clegg CH; McKnight GS
Hum Mol Genet; 1998 Jun; 7(6):959-67. PubMed ID: 9580659
[TBL] [Abstract][Full Text] [Related]
18. A Turner syndrome woman with a ring X chromosome [45,X/46,X,r(X)(p22.3q27)] whose child also had a ring X chromosome.
Uehara S; Nata M; Obara Y; Niinuma T; Funato T; Yajima A
Fertil Steril; 1997 Mar; 67(3):576-9. PubMed ID: 9091352
[TBL] [Abstract][Full Text] [Related]
19. Identification of Y-chromosomal DNA in a Turner syndrome mosaic by polymerase chain reaction.
Louie E; Nemeti M; Torfi H; Poskanzer LB; Anderson FR; Johnson JP
Ann Genet; 1991; 34(3-4):252-5. PubMed ID: 1809235
[TBL] [Abstract][Full Text] [Related]
20. Seminoma in a postmenopausal woman with a Y;15 translocation in peripheral blood lymphocytes and a t(Y;15)/45,X Turner mosaic pattern in skin fibroblasts.
Hoshi N; Fujita M; Mikuni M; Fujino T; Okuyama K; Handa Y; Yamada H; Sagawa T; Hareyama H; Nakahori Y; Fujieda K; Kant JA; Nagashima K; Fujimoto S
J Med Genet; 1998 Oct; 35(10):852-6. PubMed ID: 9783712
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]