264 related articles for article (PubMed ID: 19953489)
1. [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]
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. [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]
4. [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]
5. [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]
6. [An investigation of small marker chromosome in eight Turner syndrome patients by fluorescence in situ hybridization and DNA analysis].
Hu X; Zhu B; Hu B; Lin H; Shu D; Li C; Liu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Dec; 16(6):392-4. PubMed ID: 10581353
[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. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
9. [Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype].
Bocian E; Stańczak H; Wiśniewski A; Mazurczak T; Stankiewicz P
Pediatr Pol; 1996 Mar; 71(3):203-9. PubMed ID: 8966091
[TBL] [Abstract][Full Text] [Related]
10. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes.
Tharapel SA; Wilroy RS; Keath AM; Rivas ML; Tharapel AT
Am J Med Genet; 1992 Mar; 42(5):720-3. PubMed ID: 1632446
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Confirmation of the extra small chromosome in abnormality karyotype by PCR and FISH].
Xue ZG; Li YM; Yao ZY; Long ZG; Dai HP; Wu LQ; Xia K; Xia JH
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2005 Dec; 30(6):657-9. PubMed ID: 16708803
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. 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]
15. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
Huang Y; Sun X; Li Q
Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
[TBL] [Abstract][Full Text] [Related]
18. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
González-del-Angel A; Blanco B; del Castillo V; Carnevale A
Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
[TBL] [Abstract][Full Text] [Related]
19. [Molecular cytogenetic study of Turner's syndrome with the 45, X/46,X,r(?) karyotype].
Shi Y; Shi H; Ma S
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1994 Jun; 16(3):218-21. PubMed ID: 7805169
[TBL] [Abstract][Full Text] [Related]
20. Different chromosome Y abnormalities in Turner syndrome.
Bağci G; Acar H; Tomruk H
Genet Couns; 2001; 12(3):255-61. PubMed ID: 11693789
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
