111 related articles for article (PubMed ID: 19181594)
1. 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]
2. 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]
3. Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization.
Blennow E; Bui TH; Kristoffersson U; Vujic M; Annerén G; Holmberg E; Nordenskjöld M
Prenat Diagn; 1994 Nov; 14(11):1019-28. PubMed ID: 7877949
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.
Huang B; Solomon S; Thangavelu M; Peters K; Bhatt S
Prenat Diagn; 2006 Dec; 26(12):1142-50. PubMed ID: 17009345
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
Blennow E; Nielsen KB; Telenius H; Carter NP; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
Am J Med Genet; 1995 Jan; 55(1):85-94. PubMed ID: 7702104
[TBL] [Abstract][Full Text] [Related]
11. [Prenatal diagnosis by amniocentesis. Clinical and cytogenetic experience in 1,500 cases].
Grether-González P; Cámara-Polanco V; Ulloa-Avilés V; Salas-Labadia C; Almanza-Márquez R; Kogan-Frenk S; Kuttothara A
Ginecol Obstet Mex; 2010 Sep; 78(9):493-503. PubMed ID: 21961367
[TBL] [Abstract][Full Text] [Related]
12. [FREQUENCIES OF FETAL CHROMOSOMAL ABERRATIONS DETECTED BY AMNIOCENTESIS: OUR 15-YEARS EXPERIENCE].
Stoyanova V; Ivanov H; Linev A; Vachev T
Akush Ginekol (Sofiia); 2015; 54(5):13-8. PubMed ID: 26411190
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.
Chen CP; Chen M; Wang PT; Chern SR; Chen SW; Lai ST; Wu PS; Chang SP; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Jun; 56(3):394-397. PubMed ID: 28600058
[TBL] [Abstract][Full Text] [Related]
14. [Cytogenetical prenatal diagnosis by amniocentesis during the II and III gestation trimesters in Costa Rica].
Castro Volio I; Sander Mangel K; Vargas Prado M; Sánchez Cháves L; Escalante López G
Rev Biol Trop; 2001; 49(3-4):1227-36. PubMed ID: 12189806
[TBL] [Abstract][Full Text] [Related]
15. Clinical and cytogenetic results of a series of amniocentesis cases from Northeast China: a report of 2500 cases.
An N; Li LL; Wang RX; Li LL; Yue JM; Liu RZ
Genet Mol Res; 2015 Dec; 14(4):15660-7. PubMed ID: 26634534
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Chromosomal deletions detected at amniocentesis.
Lin CJ; Chen CP; Chien SC; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Lin KC; Yeh TT
Taiwan J Obstet Gynecol; 2014 Mar; 53(1):62-7. PubMed ID: 24767649
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.
Chen CP; Ko TM; Chen YY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Dec; 56(6):836-839. PubMed ID: 29241930
[TBL] [Abstract][Full Text] [Related]
20. Balanced reciprocal translocation at amniocentesis: cytogenetic detection and implications for genetic counseling.
Zhang HG; Zhang XY; Zhang HY; Tian T; Xu SB; Liu RZ
Genet Mol Res; 2016 Aug; 15(3):. PubMed ID: 27706592
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]