294 related articles for article (PubMed ID: 29419858)
1. [Origin and morphological features of small supernumerary marker chromosomes in Turner syndrome].
Liu N; Tong T; Chen Y; Chen Y; Cai C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):43-46. PubMed ID: 29419858
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317
[TBL] [Abstract][Full Text] [Related]
3. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
4. [Identification of the small supernumerary marker chromosomes in two patients with Turner syndrome].
Wen J; Liang D; Liao X; Xue J; Tang G; Xia Y; Long Z; Dai H; Wu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):659-63. PubMed ID: 19953489
[TBL] [Abstract][Full Text] [Related]
5. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
Liang Y; Luo XP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
[TBL] [Abstract][Full Text] [Related]
6. The clinical analysis of small supernumerary marker chromosomes in 17 children with mos 45,X/46,X,+mar karyotype.
Wang H; Wang T; Yang N; He Y; Chen L; Hong L; Shao X; Li H; Zhu H; Li H
Oncol Lett; 2017 Jun; 13(6):4385-4389. PubMed ID: 28588710
[TBL] [Abstract][Full Text] [Related]
7. Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
Sex Dev; 2007; 1(6):353-62. PubMed ID: 18391547
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.
Pietrzak J; Mrasek K; Obersztyn E; Stankiewicz P; Kosyakova N; Weise A; Cheung SW; Cai WW; von Eggeling F; Mazurczak T; Bocian E; Liehr T
J Appl Genet; 2007; 48(2):167-75. PubMed ID: 17495351
[TBL] [Abstract][Full Text] [Related]
9. Clinical and cytogenetic study of a non mosaic 46, X, isodicentric Yq in an Egyptian patient with Turner syndrome.
El-Bassyouni HT; El-Gerzawy A; Eid O; El-Ruby MO
Genet Couns; 2013; 24(1):37-44. PubMed ID: 23610863
[TBL] [Abstract][Full Text] [Related]
10. Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization.
Jang W; Chae H; Kim J; Son JO; Kim SC; Koo BK; Kim M; Kim Y; Park IY; Sung IK
Mol Cytogenet; 2016; 9():61. PubMed ID: 27508004
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
Canto P; Kofman-Alfaro S; Jiménez AL; Söderlund D; Barrón C; Reyes E; Méndez JP; Zenteno JC
Cancer Genet Cytogenet; 2004 Apr; 150(1):70-2. PubMed ID: 15041227
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Gonadoblastoma in patients with Ullrich-Turner syndrome.
Zelaya G; López Marti JM; Marino R; Garcia de Dávila MT; Gallego MS
Pediatr Dev Pathol; 2015; 18(2):117-21. PubMed ID: 25535833
[TBL] [Abstract][Full Text] [Related]
15. De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
Vundinti BR; Korgaonkar S; Ghosh K
Gene; 2012 Apr; 498(1):128-30. PubMed ID: 22342255
[TBL] [Abstract][Full Text] [Related]
16. Mosaic male fetus of Turner syndrome with partial chromosome Y: A case report.
Xue D; Cao DH; Mu K; Lv Y; Yang J
J Obstet Gynaecol Res; 2018 Jun; 44(6):1158-1162. PubMed ID: 29517175
[TBL] [Abstract][Full Text] [Related]
17. PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype.
Cervantes A; Guevara-Yáñez R; López M; Monroy N; Aguinaga M; Valdez H; Sierra C; Canún S; Guízar J; Navarrete C; Zafra G; Salamanca F; Kofman-Alfaro S
Clin Genet; 2001 Nov; 60(5):385-92. PubMed ID: 11903342
[TBL] [Abstract][Full Text] [Related]
18. Identification of marker chromosomes in thirteen patients using FISH probing.
Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
[TBL] [Abstract][Full Text] [Related]
19. [The inclusion of new techniques of chromosome analysis has improved the cytogenetic profile of Turner syndrome].
Barros BA; Maciel-Guerra AT; De Mello MP; Coeli FB; Carvalho AB; Viguetti-Campos N; Assumpção Jde G; Marques-de-Faria AP; Lemos-Marini SH; Guerra-Junior G
Arq Bras Endocrinol Metabol; 2009 Dec; 53(9):1137-42. PubMed ID: 20126871
[TBL] [Abstract][Full Text] [Related]
20. Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities.
Daggag H; Srour W; El-Khateeb M; Ajlouni K
Sex Dev; 2013; 7(6):295-302. PubMed ID: 23988405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
