135 related articles for article (PubMed ID: 33179226)
1. [Genetic analysis of three children with disorders of sex development caused by structural rearrangements of Y chromosome].
Wang H; Chen L; Chen Y; Shen Y; Li L; Shao X; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1226-1232. PubMed ID: 33179226
[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. [Genetic analysis for a female carrying idic(Y)(p11.32) with Disorders of sex development].
Zhang Y; Xu Z; Zhao X; Li L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):626-631. PubMed ID: 38684314
[TBL] [Abstract][Full Text] [Related]
4. [Clinical and genetic characteristic in patients with disorders of sex development caused by Y chromosome copy number variant].
Xia JK; Tian FY; Hou YQ; Zhao YJ; Kong XD
Zhonghua Er Ke Za Zhi; 2023 May; 61(5):459-463. PubMed ID: 37096267
[No Abstract] [Full Text] [Related]
5. [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]
6. 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]
7. Translocation (Y;22) resulting in the loss of SHOX and isolated short stature.
Borie C; Léger J; Dupuy O; Hassan M; Ledu N; Lebbar A; Czernichow P; Eydoux P
Am J Med Genet A; 2004 Mar; 125A(2):186-90. PubMed ID: 14981722
[TBL] [Abstract][Full Text] [Related]
8. Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions.
Jorgez CJ; Weedin JW; Sahin A; Tannour-Louet M; Han S; Bournat JC; Mielnik A; Cheung SW; Nangia AK; Schlegel PN; Lipshultz LI; Lamb DJ
J Clin Endocrinol Metab; 2011 Apr; 96(4):E674-9. PubMed ID: 21252244
[TBL] [Abstract][Full Text] [Related]
9. [Prenatal diagnosis for two fetuses carrying partial deletion of Y chromosome].
Pang H; Gao M; Hua J; Tong D; Zhao Y; Feng X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb; 37(2):182-185. PubMed ID: 32034751
[TBL] [Abstract][Full Text] [Related]
10. Molecular and clinical characteristics of 26 cases with structural Y chromosome aberrations.
Kim JW; Park SY; Ryu HM; Lee DE; Lee BY; Kim SY; Park YS; Lee HS; Seo JT
Cytogenet Genome Res; 2012; 136(4):270-7. PubMed ID: 22688216
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Prenatal diagnosis of sex chromosomal inversion, translocation and deletion.
Zhang L; Ren M; Song G; Zhang Y; Liu X; Zhang X; Wang J
Mol Med Rep; 2018 Feb; 17(2):2811-2816. PubMed ID: 29257243
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. 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]
16. 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]
17. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
Tatar A; Oztas S; Yakut T; Ors R
Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221).
Clement A; Dominot T; Chammas J; Montagnon M; Delcroix M; Pfeffer J; Dupont JM; Lebbar A; Clement P; Vialard F
Genes (Basel); 2022 Dec; 14(1):. PubMed ID: 36672822
[TBL] [Abstract][Full Text] [Related]
20. [Prenatal diagnosis and genetic analysis of a fetus with der(X)t(X;Y)(p22.3;q11.2)].
Li J; Dong Y; Li J; Luo J; Li C; Qi H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1287-1290. PubMed ID: 33179242
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
