118 related articles for article (PubMed ID: 11415513)
41. Turner syndrome diagnosed in northeastern Malaysia.
Kannan TP; Azman BZ; Ahmad Tarmizi AB; Suhaida MA; Siti Mariam I; Ravindran A; Zilfalil BA
Singapore Med J; 2008 May; 49(5):400-4. PubMed ID: 18465051
[TBL] [Abstract][Full Text] [Related]
42. 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]
43. X inactivation Xplained.
Wutz A; Gribnau J
Curr Opin Genet Dev; 2007 Oct; 17(5):387-93. PubMed ID: 17869504
[TBL] [Abstract][Full Text] [Related]
44. Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: implications for prenatal counseling and estrogen therapy at puberty.
Blair J; Tolmie J; Hollman AS; Donaldson MD
J Pediatr; 2001 Nov; 139(5):724-8. PubMed ID: 11713453
[TBL] [Abstract][Full Text] [Related]
45. Different chromosome Y abnormalities in Turner syndrome.
Bağci G; Acar H; Tomruk H
Genet Couns; 2001; 12(3):255-61. PubMed ID: 11693789
[TBL] [Abstract][Full Text] [Related]
46. A phenotypically normal female with pseudodicentric X: correlation for statural genes.
Gole LA; Annapoorna V; Lim J; Anandakumar C
Singapore Med J; 2001 Sep; 42(9):428-9. PubMed ID: 11811611
[TBL] [Abstract][Full Text] [Related]
47. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
Huang Y; Sun X; Li Q
Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
[TBL] [Abstract][Full Text] [Related]
48. X chromosomal abnormalities in Indian adolescent girls.
Ganguly BB; Sahni S
Teratog Carcinog Mutagen; 2003; Suppl 1():245-53. PubMed ID: 12616615
[TBL] [Abstract][Full Text] [Related]
49. Chromosomal mosaicism mitigates stigmata and cardiovascular risk factors in Turner syndrome.
El-Mansoury M; Barrenäs ML; Bryman I; Hanson C; Larsson C; Wilhelmsen L; Landin-Wilhelmsen K
Clin Endocrinol (Oxf); 2007 May; 66(5):744-51. PubMed ID: 17381484
[TBL] [Abstract][Full Text] [Related]
50. Isochromosome Xq in mosaicism with a cell line with two normal X-chromosomes: association with psychomotor retardation and neurological deficit.
Fryns JP; Kleczkowska A; Van den Berghe H
Ann Genet; 1993; 36(3):173-5. PubMed ID: 8117065
[No Abstract] [Full Text] [Related]
51. 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]
52. 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]
53. Analysis of the SRY gene in a girl with 45,X/46,XY genotype.
Akbas E; Soylemez F; Hallioglu O; Polat S; Turkoz G
Genet Couns; 2009; 20(3):249-54. PubMed ID: 19852431
[TBL] [Abstract][Full Text] [Related]
54. Turner syndrome and 45,X/47,XXX mosaicism.
Akbas E; Mutluhan H; Savasoglu K; Soylemez F; Ozturk I; Yazici G
Genet Couns; 2009; 20(2):141-6. PubMed ID: 19650411
[TBL] [Abstract][Full Text] [Related]
55. Aberrant patterns of X chromosome inactivation in bovine clones.
Xue F; Tian XC; Du F; Kubota C; Taneja M; Dinnyes A; Dai Y; Levine H; Pereira LV; Yang X
Nat Genet; 2002 Jun; 31(2):216-20. PubMed ID: 12032569
[TBL] [Abstract][Full Text] [Related]
56. Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location.
Boucher CA; Sargent CA; Ogata T; Affara NA
J Med Genet; 2001 Sep; 38(9):591-8. PubMed ID: 11546827
[TBL] [Abstract][Full Text] [Related]
57. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
Zhu XY; Zhao R; Ye ZC; Peng YG; Tan YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Study on the relationship between cytogenetics and phenotypic effect in Turner's syndrome.
Hu X; Zhu B; Lin H; Shu D; Tao D; Wang M
J Tongji Med Univ; 1996; 16(4):245-8. PubMed ID: 9389092
[TBL] [Abstract][Full Text] [Related]
60. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT
Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
