These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
133 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. [Genetic analysis of a fetus with with 45,X/46,X,idic(Y)(q11.2) mosaicism]. Pan F; Zhang W; Zhang W Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug; 41(8):897-902. PubMed ID: 39097269 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. 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]
9. 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]
10. [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]
11. 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]
12. 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]
13. 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]
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. 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]
18. 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]
19. 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]
20. 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] [Next] [New Search]