205 related articles for article (PubMed ID: 20570968)
1. Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.
Scott SA; Cohen N; Brandt T; Warburton PE; Edelmann L
Hum Mol Genet; 2010 Sep; 19(17):3383-93. PubMed ID: 20570968
[TBL] [Abstract][Full Text] [Related]
2. [Prenatal diagnosis and genetic analysis of two cases of Turner syndrome due to isodicentric Xp11.22].
Wang L; Kang H; Hu Y; Wu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar; 40(3):368-373. PubMed ID: 36854417
[TBL] [Abstract][Full Text] [Related]
3. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
Reshmi SC; Miller JL; Deplewski D; Close C; Henderson LJ; Littlejohn E; Schwartz S; Waggoner DJ
Eur J Med Genet; 2011; 54(2):161-4. PubMed ID: 21078420
[TBL] [Abstract][Full Text] [Related]
4. Correlation of intercentromeric distance, mosaicism, and sexual phenotype: molecular localization of breakpoints in isodicentric Y chromosomes.
Beaulieu Bergeron M; Brochu P; Lemyre E; Lemieux N
Am J Med Genet A; 2011 Nov; 155A(11):2705-12. PubMed ID: 21964771
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of an idic(Y)(qter -->p11.32::p11.32-->qter) chromosome from a female patient with a complex karyotype.
Fernandez R; Pasaro E
Genet Mol Res; 2006 Jun; 5(2):399-406. PubMed ID: 16819718
[TBL] [Abstract][Full Text] [Related]
6. Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination.
Lebo RV; Milunsky J; Higgins AW; Loose B; Huang XL; Wyandt HE
Am J Med Genet; 1999 Aug; 85(5):429-37. PubMed ID: 10405438
[TBL] [Abstract][Full Text] [Related]
7. Left-sided congenital heart lesions in mosaic Turner syndrome.
Bouayed Abdelmoula N; Abdelmoula B; Smaoui W; Trabelsi I; Louati R; Aloulou S; Aloulou W; Abid F; Kammoun S; Trigui K; Bedoui O; Denguir H; Mallek S; Ben Aziza M; Dammak J; Kaabi O; Abdellaoui N; Turki F; Kaabi A; Kamoun W; Jabeur J; Ltaif W; Chaker K; Fourati H; M'rabet S; Ben Ameur H; Gouia N; Mhiri MN; Rebai T
Mol Genet Genomics; 2018 Apr; 293(2):495-501. PubMed ID: 29196848
[TBL] [Abstract][Full Text] [Related]
8. Fine mapping of an isodicentric Y chromosomal breakpoint from a schizophrenic patient.
Yoshitsugu K; Meerabux JM; Asai K; Yoshikawa T
Am J Med Genet B Neuropsychiatr Genet; 2003 Jan; 116B(1):27-31. PubMed ID: 12497609
[TBL] [Abstract][Full Text] [Related]
9. Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
McDonell N; Ramser J; Francis F; Vinet MC; Rider S; Sudbrak R; Riesselman L; Yaspo ML; Reinhardt R; Monaco AP; Ross F; Kahn A; Kearney L; Buckle V; Chelly J
Genomics; 2000 Mar; 64(3):221-9. PubMed ID: 10756090
[TBL] [Abstract][Full Text] [Related]
10. Isodicentric Y chromosomes in Egyptian patients with disorders of sex development (DSD).
Mekkawy M; Kamel A; El-Ruby M; Mohamed A; Essawi M; Soliman H; Dessouky N; Shehab M; Mazen I
Am J Med Genet A; 2012 Jul; 158A(7):1594-603. PubMed ID: 22628100
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic and molecular characterization of two isodicentric Y chromosomes.
Stankiewicz P; Hélias-Rodzewicz Z; Jakubów-Durska K; Bocian E; Obersztyn E; Rappold GA; Mazurczak T
Am J Med Genet; 2001 Jun; 101(1):20-5. PubMed ID: 11343332
[TBL] [Abstract][Full Text] [Related]
12. Mixed gonadal dysgenesis in a child with isodicentric Y chromosome: Does the relative proportion of the 45,X line really matter?
Shinawi M; Cain MP; Vanderbrink BA; Grignon DJ; Mensing D; Cooper ML; Bader P; Cheung SW
Am J Med Genet A; 2010 Jul; 152A(7):1832-7. PubMed ID: 20583182
[TBL] [Abstract][Full Text] [Related]
13. Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations.
Nothwang HG; Schröer A; van der Maarel S; Kübart S; Schneider S; Riesselmann L; Menzel C; Hinzmann B; Vogt D; Rosenthal A; Fryns J; Tommerup N; Haaf T; Ropers HH; Wirth J
Cytogenet Cell Genet; 2000; 90(1-2):126-33. PubMed ID: 11060462
[TBL] [Abstract][Full Text] [Related]
14. Familial occurrence of isodicentric X chromosomes with different breakpoints.
Midro AT; Kulikowski M; Sawicka A; Panasiuk B; Korsak E
Clin Genet; 1988 Sep; 34(3):153-60. PubMed ID: 3180502
[TBL] [Abstract][Full Text] [Related]
15. Early recurrence in standard-risk medulloblastoma patients with the common idic(17)(p11.2) rearrangement.
Bien-Willner GA; López-Terrada D; Bhattacharjee MB; Patel KU; Stankiewicz P; Lupski JR; Pfeifer JD; Perry A
Neuro Oncol; 2012 Jul; 14(7):831-40. PubMed ID: 22573308
[TBL] [Abstract][Full Text] [Related]
16. De novo isodicentric X chromosome: 46,X,idic(X)(q24), and summary of literature.
Tsai AC; Fine CA; Yang M; Walton CS; Beischel L; Johnson JP
Am J Med Genet A; 2006 Apr; 140(8):923-30. PubMed ID: 16528747
[TBL] [Abstract][Full Text] [Related]
17. [Screening for Y chromosome sequences in patients with Turner syndrome].
Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
[TBL] [Abstract][Full Text] [Related]
18. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype.
Al-Achkar W; Wafa A; Liehr T; Klein E; Moassass F
Mol Med Rep; 2012 Aug; 6(2):293-6. PubMed ID: 22664581
[TBL] [Abstract][Full Text] [Related]
19. Clinical, cytogenomic, and molecular characterization of isodicentric Y-chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and severe oligozoospermic infertile men.
Abur U; Gunes S; Hekim N; Akar OS; Altundag E; Asci R
J Assist Reprod Genet; 2022 Dec; 39(12):2799-2810. PubMed ID: 36251127
[TBL] [Abstract][Full Text] [Related]
20. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
Aktas D; Alikasifoglu M; Gonc N; Senocak ME; Tuncbilek E
Eur J Med Genet; 2006; 49(2):141-9. PubMed ID: 16530711
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]