237 related articles for article (PubMed ID: 12533818)
1. The clinical application of spectral karyotyping (SKY) in the analysis of prenatally diagnosed extra structurally abnormal chromosomes (ESACs).
Yaron Y; Carmon E; Goldstein M; Voskoboinik N; Ochshorn Y; Gelman-Kohan Z; Orr-Urtreger A
Prenat Diagn; 2003 Jan; 23(1):74-9. PubMed ID: 12533818
[TBL] [Abstract][Full Text] [Related]
2. Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up.
Marchina E; Piovani G; Vezzola L; Bellotti D; Cerri V; Groli C; Barlati S
Prenat Diagn; 2003 Dec; 23(12):959-63. PubMed ID: 14663830
[TBL] [Abstract][Full Text] [Related]
3. Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature.
Hastings RJ; Nisbet DL; Waters K; Spencer T; Chitty LS
Prenat Diagn; 1999 May; 19(5):436-45. PubMed ID: 10360512
[TBL] [Abstract][Full Text] [Related]
4. [Spectral karyotyping of seven prenatally detected marker chromosomes and complex chromosome aberrations].
Song HL; Chen BJ; Fang Q; Xie YJ; Lin SB; Wu JZ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):393-7. PubMed ID: 22875493
[TBL] [Abstract][Full Text] [Related]
5. [Application of spectral karyotyping in diagnosis of complex chromosome aberration].
Pan M; Liao C; Li DZ; Yi CX; Yuan SM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):474-6. PubMed ID: 17680548
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of extrastructurally abnormal chromosomes: clinical experience and literature review.
Tseng JJ; Chou MM; Lo FC; Lai HY; Chen MH; Ho ES
J Chin Med Assoc; 2009 Jan; 72(1):29-33. PubMed ID: 19181594
[TBL] [Abstract][Full Text] [Related]
9. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.
Michalski K; Rauer M; Williamson N; Perszyk A; Hoo JJ
Am J Med Genet; 1993 Apr; 46(1):88-94. PubMed ID: 8494036
[TBL] [Abstract][Full Text] [Related]
10. Prenatally diagnosed balanced chromosome rearrangements: eight years' experience.
Peng HH; Chao AS; Wang TH; Chang YL; Chang SD
J Reprod Med; 2006 Sep; 51(9):699-703. PubMed ID: 17039698
[TBL] [Abstract][Full Text] [Related]
11. [The clinical application of spectral karyotyping in the analysis of chromosomal abnormalities].
Guo QS; Zhang YP; Li XT; Han JL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):80-3. PubMed ID: 17285551
[TBL] [Abstract][Full Text] [Related]
12. Extra structurally abnormal chromosomes (ESACs)--presentation of 10 new cases.
Kałuzewski B; Helszer Z; Constantinou M; Burkholder SW; Coutinho WG; Skorski M; Corridori L; Anderson CE; Sherwood M; Debiec-Rychter M; Jackson LG
Med Sci Monit; 2001; 7(3):427-34. PubMed ID: 11386020
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
[TBL] [Abstract][Full Text] [Related]
14. Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis.
Calabrese G; Stuppia L; Mingarelli R; Guanciali Franchi P; Peila R; Morizio E; Antonucci A; Palka G
Ann Genet; 1994; 37(3):135-8. PubMed ID: 7847794
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Spectral karyotyping (SKY) principle, avantages and limitations].
Belaud-Rotureau MA; Elghezal H; Bernardin C; Sanlaville D; Radford-Weiss I; Raoul O; Vekemans M; Romana SP
Ann Biol Clin (Paris); 2003; 61(2):139-46. PubMed ID: 12702468
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16.
Yakut S; Cetin Z; Simşek M; Karaüzüm SB; Tükün A; Lüleci G
Genet Couns; 2009; 20(4):327-32. PubMed ID: 20162867
[TBL] [Abstract][Full Text] [Related]
18. Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY).
Cohen N; Betts DR; Trakhtenbrot L; Niggli FK; Amariglio N; Brok-Simoni F; Rechavi G; Meitar D
Genes Chromosomes Cancer; 2001 Jul; 31(3):201-8. PubMed ID: 11391790
[TBL] [Abstract][Full Text] [Related]
19. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
Mercier S; Fellmann F; Cattin J; Bresson JL
Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640
[TBL] [Abstract][Full Text] [Related]
20. Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.
Lebbar A; Viot G; Szpiro-Tapia S; Baverel F; Rabineau D; Dupont JM
Prenat Diagn; 2002 Nov; 22(11):973-5. PubMed ID: 12424758
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]