152 related articles for article (PubMed ID: 18925662)
21. 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]
22. A unique patient with an Ullrich-Turner syndrome variant and mosaicism for a tiny r(X) and a partial proximal duplication 1q.
Dawson AJ; Wickstrom DE; Riordan D; Cardwell S; Casey R; Baldry S; Brown C
Am J Med Genet A; 2004 Jan; 124A(3):303-6. PubMed ID: 14708105
[TBL] [Abstract][Full Text] [Related]
23. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
[TBL] [Abstract][Full Text] [Related]
24. Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X.
González-Rodríguez MTA; Brukman-Jiménez SA; Cuero-Quezada I; Corona-Rivera JR; Corona-Rivera A; Serafín-Saucedo G; Aguirre-Salas LM; Bobadilla-Morales L
Genes (Basel); 2023 Jan; 14(2):. PubMed ID: 36833181
[TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis of a small supernumerary, XIST-negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetus.
Le Caignec C; Boceno M; Joubert M; Winer N; Aubron F; Fallet-Bianco C; Rival JM
Prenat Diagn; 2003 Feb; 23(2):143-5. PubMed ID: 12575022
[TBL] [Abstract][Full Text] [Related]
26. Prune-belly syndrome and other anomalies in a stillborn fetus with a ring X chromosome lacking XIST.
Guillén DR; Lowichik A; Schneider NR; Cohen DS; Garcia S; Zinn AR
Am J Med Genet; 1997 May; 70(1):32-6. PubMed ID: 9129738
[TBL] [Abstract][Full Text] [Related]
27. Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.
Callen DF; Eyre HJ; Dolman G; Garry-Battersby MB; McCreanor JR; Valeba A; McGill JJ
J Med Genet; 1995 Feb; 32(2):113-6. PubMed ID: 7760319
[TBL] [Abstract][Full Text] [Related]
28. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
29. Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.
Schluth C; Cossée M; Girard-Lemaire F; Carelle N; Dollfus H; Jeandidier E; Flori E
Pathol Biol (Paris); 2007 Feb; 55(1):29-36. PubMed ID: 16690229
[TBL] [Abstract][Full Text] [Related]
30. A boy with small supernumerary marker chromosome X identified by FISH.
Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
Wolff DJ; Brown CJ; Schwartz S; Duncan AM; Surti U; Willard HF
Am J Hum Genet; 1994 Jul; 55(1):87-95. PubMed ID: 8023855
[TBL] [Abstract][Full Text] [Related]
33. The Turner syndrome life course project: Karyotype-phenotype analyses across the lifespan.
Cameron-Pimblett A; La Rosa C; King TFJ; Davies MC; Conway GS
Clin Endocrinol (Oxf); 2017 Nov; 87(5):532-538. PubMed ID: 28617979
[TBL] [Abstract][Full Text] [Related]
34. [Turner's syndrome--correlation between karyotype and phenotype].
Lacka K
Endokrynol Pol; 2005; 56(6):986-93. PubMed ID: 16821224
[TBL] [Abstract][Full Text] [Related]
35. Mosaic male fetus of Turner syndrome with partial chromosome Y: A case report.
Xue D; Cao DH; Mu K; Lv Y; Yang J
J Obstet Gynaecol Res; 2018 Jun; 44(6):1158-1162. PubMed ID: 29517175
[TBL] [Abstract][Full Text] [Related]
36. Genetic considerations in the patient with Turner syndrome--45,X with or without mosaicism.
Zhong Q; Layman LC
Fertil Steril; 2012 Oct; 98(4):775-9. PubMed ID: 23020909
[TBL] [Abstract][Full Text] [Related]
37. Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes.
Migeon BR; Luo S; Stasiowski BA; Jani M; Axelman J; Van Dyke DL; Weiss L; Jacobs PA; Yang-Feng TL; Wiley JE
Proc Natl Acad Sci U S A; 1993 Dec; 90(24):12025-9. PubMed ID: 8265665
[TBL] [Abstract][Full Text] [Related]
38. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.
Jenderny J; Caliebe A; Beyer C; Grote W
J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656
[TBL] [Abstract][Full Text] [Related]
39. Ring chromosome X in a child with manifestations of Kabuki syndrome.
McGinniss MJ; Brown DH; Burke LW; Mascarello JT; Jones MC
Am J Med Genet; 1997 May; 70(1):37-42. PubMed ID: 9129739
[TBL] [Abstract][Full Text] [Related]
40. Severe phenotypes associated with inactive ring X chromosomes.
Migeon BR; Ausems M; Giltay J; Hasley-Royster C; Kazi E; Lydon TJ; Engelen JJ; Raymond GV
Am J Med Genet; 2000 Jul; 93(1):52-7. PubMed ID: 10861682
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]