233 related articles for article (PubMed ID: 26829740)
1. [Cytogenetic and molecular genetic analysis of a case with mosaic marker chromosomes].
Tu X; Zeng J; Cong X; Zhang X; Yan A
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):76-80. PubMed ID: 26829740
[TBL] [Abstract][Full Text] [Related]
2. [Delineation of three structural Y chromosome aberrations combined molecular techniques].
Tu XD; Zeng J; Cong XW; Yan AZ; Huang WJ; Lin YH; Zheng DZ; Zhang M; Wang ZH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):420-4. PubMed ID: 23926008
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of sex chromosome mosaicism with two marker chromosomes in three cell lines and a review of the literature.
Zheng J; Yang X; Lu H; Guan Y; Yang F; Xu M; Li M; Ji X; Wang Y; Hu P; Zhou Y
Mol Med Rep; 2019 Mar; 19(3):1791-1796. PubMed ID: 30592288
[TBL] [Abstract][Full Text] [Related]
4. Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.
Castro A; Rodríguez F; Flórez M; López P; Curotto B; Martínez D; Maturana A; Lardone MC; Palma C; Mericq V; Ebensperger M; Cassorla F
Hum Reprod; 2017 Feb; 32(2):465-475. PubMed ID: 28057878
[TBL] [Abstract][Full Text] [Related]
5. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
Hernando C; Carrera M; Ribas I; Parear N; Baraibar R; Egocue J; Fuster C
Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
[TBL] [Abstract][Full Text] [Related]
6. [Cytogenetics and Y chromosome AZF microdeletions in infertile patients with mosaic karyotype Klinefelter syndrome (46,XY/47,XXY/48, XXYY/49,XXXXY)].
Tian L; Zhang JW; Shen CX; Du Y; Zhou X
Zhonghua Nan Ke Xue; 2012 Jun; 18(6):545-50. PubMed ID: 22774613
[TBL] [Abstract][Full Text] [Related]
7. Hypospadias in a male infant with an unusual mosaic 45,X/46,X,psu idic(Y)(p11.32)/46,XY and haploinsufficiency of SHOX: A case report.
Si YM; Dong Y; Wang W; Qi KY; Wang X
Mol Med Rep; 2017 Jul; 16(1):201-207. PubMed ID: 28498391
[TBL] [Abstract][Full Text] [Related]
8. [Positioning analysis of the Yq11 deletion in a patient with azoospermia].
Tu XO; Lan FU; Zhu ZO
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):203-5. PubMed ID: 18393247
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Cytogenetic and molecular study of a patient with severe oligozoospermia and asthenozoospermia].
Lin S; Xie Y; Wu J; Fang Q; Chen Z; Chen B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):65-8. PubMed ID: 24510566
[TBL] [Abstract][Full Text] [Related]
11. Identification of the origin of marker chromosomes by two-color fluorescence in situ hybridization and polymerase chain reaction in azoospermic patients.
Wei CL; Cheng JL; Yang WC; Li LY; Cheng HC; Fu JJ
Genet Mol Res; 2015 Nov; 14(4):14488-95. PubMed ID: 26600507
[TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.
Bettio D; Venci A; Rizzi N; Negri L; Setti PL
Hum Reprod; 2006 Apr; 21(4):972-5. PubMed ID: 16484313
[TBL] [Abstract][Full Text] [Related]
13. [Investigation of a rare supernumerary i(Y)(q10) chromosome in a patient with premature ovarian failure].
Zeng H; Kong H; Xiao Y; Huang T; Wu H; Shen Y; Zhou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):192-5. PubMed ID: 24711030
[TBL] [Abstract][Full Text] [Related]
14. [Y-chromosome microdeletions as a prognostic marker of male infertility].
Tyrkus MIa; Makukh HV; Zastavna DV; Huleiuk NL; Nakonechnyĭ AI; Stoĭka BR
Tsitol Genet; 2008; 42(2):46-50. PubMed ID: 18630120
[TBL] [Abstract][Full Text] [Related]
15. [Genetic analysis for 2 females carrying idic(Y)(p) and with sex development disorders].
Zhang Y; Wang H; Jia Z; Hu J; Cao W; Tan Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):335-9. PubMed ID: 27264816
[TBL] [Abstract][Full Text] [Related]
16. 47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formation.
Pasantes JJ; Wimmer R; Knebel S; Münch C; Kelbova C; Junge A; Kieback P; Küpferling P; Schempp W
Cytogenet Genome Res; 2012; 136(2):157-62. PubMed ID: 22286088
[TBL] [Abstract][Full Text] [Related]
17. Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive.
Wu QY; Li N; Li WW; Li TF; Zhang C; Cui YX; Xia XY; Zhai JS
BMC Urol; 2014 Aug; 14():70. PubMed ID: 25169080
[TBL] [Abstract][Full Text] [Related]
18. Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome.
He S; Xi H; Chen J; Wang D; Pang J; Hu J; Liu Q; Jia Z; Wang H
Mol Cytogenet; 2020; 13():7. PubMed ID: 32071615
[TBL] [Abstract][Full Text] [Related]
19. Detailed analysis of isodicentric Y in a case with azoospermia and 45,x/46,x,idic(Y) mosaicism.
Lee J; Park JK; Kim DS; Lee HS; Choi SI; Cho YG
Ann Clin Lab Sci; 2015; 45(2):206-8. PubMed ID: 25887877
[TBL] [Abstract][Full Text] [Related]
20. Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul D; Attanasio L; Oehler E; Hamosh A; Blakemore K; Stetten G
Prenat Diagn; 2007 Apr; 27(4):373-9. PubMed ID: 17286317
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
