183 related articles for article (PubMed ID: 33751538)
1. [Cytogenetic and molecular genetic analysis of three cases with small supernumerary marker chromosomes].
Fan J; Zeng Y; Luo T; Che M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):264-267. PubMed ID: 33751538
[TBL] [Abstract][Full Text] [Related]
2. [Cytogenetic and molecular genetic analysis of small supernumerary marker chromosomes in fetal amniotic fluid].
Zhang W; Pan Y; Zhang Y; Dai M; Chen X; Shi W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):187-191. PubMed ID: 28397215
[TBL] [Abstract][Full Text] [Related]
3. [Genetic analysis and assisted reproductive guidance for two infertile patients with rare small supernumerary marker chromosomes].
Yi D; Yuan S; Hu L; Gong F; Luo K; Hu H; Tan Y; Lu G; Lin G; Cheng D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):519-525. PubMed ID: 38684294
[TBL] [Abstract][Full Text] [Related]
4. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
[TBL] [Abstract][Full Text] [Related]
5. The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.
Karaman B; Aytan M; Yilmaz K; Toksoy G; Onal EP; Ghanbari A; Engur A; Kayserili H; Yuksel-Apak M; Basaran S
Eur J Med Genet; 2006; 49(3):207-14. PubMed ID: 16762822
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis.
Xue H; Chen X; Lin M; Lin N; Huang H; Yu A; Xu L
Aging (Albany NY); 2020 Dec; 13(2):2135-2148. PubMed ID: 33318309
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report.
Sun M; Wang R; Zhang H; Jiang Y; He J; Li S; Liu R
Exp Ther Med; 2020 Apr; 19(4):2927-2932. PubMed ID: 32256778
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Lai ST; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616
[TBL] [Abstract][Full Text] [Related]
10. [Study of two cases of prenatally detected small supernumerary marker chromosomes].
Zeng Y; Fan J; Xu P; Zhang L; Qian F; Luo T
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):498-500. PubMed ID: 27455006
[TBL] [Abstract][Full Text] [Related]
11. [Identification of human small supernumerary marker chromosomes and discussion of its research value].
Ou J; Wang W; Duan CY; Fu WY; Liu YL; Sun J; Zhong HL; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):91-4. PubMed ID: 23450489
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review.
Sun ML; Zhang HG; Liu XY; Yue FG; Jiang YT; Li SB; Liu RZ
Taiwan J Obstet Gynecol; 2020 Nov; 59(6):963-967. PubMed ID: 33218423
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Delineation of a mosaicism fetal supernumerary marker chromosome with combined genetic techniques].
Lu J; Lu J; Qin H; Ye X; Qiu J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Oct; 40(10):1296-1300. PubMed ID: 37730235
[TBL] [Abstract][Full Text] [Related]
17. [Application of single nucleotide polymorphism microarray and fluorescence in situ hybridization analysis for the prenatal diagnosis of a case with Pallister-Killian syndrome].
Zhang W; Guo Z; Wang W; Sun Y; Zhang C; Wang X; Zhang L; Wang C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):232-235. PubMed ID: 29652999
[TBL] [Abstract][Full Text] [Related]
18. [Prenatal diagnosis of a fetus with two small supernumerary marker chromosomes].
Zhang J; Jiang Y; Cai M; Ge Y; Zhou Y; Wang W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1222-1225. PubMed ID: 31813153
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
