140 related articles for article (PubMed ID: 20117774)
41. Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis.
Gole LA; Lim J; Crolla JA; Loke KY
Singapore Med J; 2008 Apr; 49(4):349-51. PubMed ID: 18418530
[TBL] [Abstract][Full Text] [Related]
42. [45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12) mosaicism in a female patient with gonadal dysgenesis and the stigmata of Turner's syndrome].
Gil R; Galán F; López-Ginés C; Gregori-Romero M; Millet A; Pellín A; Llombart-Bosch A
Rev Clin Esp; 1991 Jun; 189(1):23-5. PubMed ID: 1924922
[TBL] [Abstract][Full Text] [Related]
43. H-Y antigen in XO/X,iso(X) mosaic Turner syndrome.
Meade KW; Wachtel SS; Davis JR; Lightner ES
Obstet Gynecol; 1981 May; 57(5):594-9. PubMed ID: 7194461
[TBL] [Abstract][Full Text] [Related]
44. Genomic imprinting in Turner syndrome: effects on response to growth hormone and on risk of sensorineural hearing loss.
Hamelin CE; Anglin G; Quigley CA; Deal CL
J Clin Endocrinol Metab; 2006 Aug; 91(8):3002-10. PubMed ID: 16757526
[TBL] [Abstract][Full Text] [Related]
45. [Clinical picture in patients with 46,X,i(Xq) karyotype. Are there differences from Turner syndrome?].
Holzgreve W; Herbst J
Zentralbl Gynakol; 1985; 107(14):863-8. PubMed ID: 3839961
[TBL] [Abstract][Full Text] [Related]
46. An atypical Turner syndrome patient with ring X chromosome mosaicism.
Cantú ES; Jacobs DF; Pai GS
Ann Clin Lab Sci; 1995; 25(1):60-5. PubMed ID: 7762970
[TBL] [Abstract][Full Text] [Related]
47. Lack of X inactivation: loss of one X inactivation center in a case with mos45,X,-21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2).
Ishikiriyama S; Iai M; Tanabe Y
Am J Med Genet; 1993 Aug; 47(1):41-4. PubMed ID: 8368250
[TBL] [Abstract][Full Text] [Related]
48. [Y chromosome structural abnormalities and Turner's syndrome].
Ravel C; Siffroi JP
Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
[TBL] [Abstract][Full Text] [Related]
49. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S
Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415
[TBL] [Abstract][Full Text] [Related]
50. Parental origin and mechanism of formation of X chromosome structural abnormalities: four cases determined with RFLPs.
Deng HX; Xia JH; Ishikawa M; Niikawa N
Jinrui Idengaku Zasshi; 1990 Sep; 35(3):245-51. PubMed ID: 1979996
[TBL] [Abstract][Full Text] [Related]
51. Apparent neotelomere in a 46,X,del(X)(qter→p11.2:)/46,X,rea(X)(qter→p11.2::q21.2→qter) novel mosaicism: review of 34 females with a recombinant-like dup(Xq) chromosome.
Vásquez-Velásquez AI; Torres-Flores J; Leal CA; Rivera H
Genet Test Mol Biomarkers; 2011 Oct; 15(10):727-31. PubMed ID: 21651320
[TBL] [Abstract][Full Text] [Related]
52. [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]
53. Shox and Awe: A Case of Variant Turner Syndrome with an Unusual Phenotype.
LaValley C; Devitt K; Gardner JA
J Assoc Genet Technol; 2019; 45(1):18-20. PubMed ID: 30840602
[TBL] [Abstract][Full Text] [Related]
54. Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients.
Ogata T; Muroya K; Matsuo N; Shinohara O; Yorifuji T; Nishi Y; Hasegawa Y; Horikawa R; Tachibana K
J Clin Endocrinol Metab; 2001 Nov; 86(11):5498-508. PubMed ID: 11701728
[TBL] [Abstract][Full Text] [Related]
55. Functional disomy of Xp: prenatal findings and postnatal outcome.
Kolomietz E; Godbole K; Winsor EJ; Stockley T; Seaward G; Chitayat D
Am J Med Genet A; 2005 May; 134(4):393-8. PubMed ID: 15793841
[TBL] [Abstract][Full Text] [Related]
56. Cytogenetics findings at Turner Syndrome and their correlation with clinical findings.
Catović A
Bosn J Basic Med Sci; 2005 Aug; 5(3):54-8. PubMed ID: 16351583
[TBL] [Abstract][Full Text] [Related]
57. Clinical significance of the parental origin of the X chromosome in turner syndrome.
Sagi L; Zuckerman-Levin N; Gawlik A; Ghizzoni L; Buyukgebiz A; Rakover Y; Bistritzer T; Admoni O; Vottero A; Baruch O; Fares F; Malecka-Tendera E; Hochberg Z
J Clin Endocrinol Metab; 2007 Mar; 92(3):846-52. PubMed ID: 17192299
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature.
Ogata T; Kosho T; Wakui K; Fukushima Y; Yoshimoto M; Miharu N
J Clin Endocrinol Metab; 2000 Aug; 85(8):2927-30. PubMed ID: 10946905
[TBL] [Abstract][Full Text] [Related]
60. Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes.
Monroy N; López M; Cervantes A; García-Cruz D; Zafra G; Canún S; Zenteno JC; Kofman-Alfaro S
Am J Med Genet; 2002 Jan; 107(3):181-9. PubMed ID: 11807897
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]