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Results: 1 to 20 of 213

1.

Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.

Mademont-Soler I, Morales C, Soler A, Martínez-Crespo JM, Shen Y, Margarit E, Clusellas N, Obón M, Wu BL, Sánchez A.

Ultrasound Obstet Gynecol. 2013 Apr;41(4):375-82. doi: 10.1002/uog.12372. Epub 2013 Mar 4.

PMID:
23233332
[PubMed - indexed for MEDLINE]
Free Article
2.

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.

Fiorentino F, Napoletano S, Caiazzo F, Sessa M, Bono S, Spizzichino L, Gordon A, Nuccitelli A, Rizzo G, Baldi M.

Eur J Hum Genet. 2013 Jul;21(7):725-30. doi: 10.1038/ejhg.2012.253. Epub 2012 Dec 5.

PMID:
23211699
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study.

Schmid M, Stary S, Springer S, Bettelheim D, Husslein P, Streubel B.

Ultrasound Obstet Gynecol. 2013 Mar;41(3):267-73. doi: 10.1002/uog.12389.

PMID:
23292918
[PubMed - indexed for MEDLINE]
Free Article
4.

[Clinical features of abnormal chromosome karyotypes in twin pregnancies complicated with structural abnormalities].

Zhong SL, Fang Q, Chen BJ, Han ZY, Luo YM, Chen JS, Xie YJ.

Zhonghua Fu Chan Ke Za Zhi. 2011 Sep;46(9):649-54. Chinese.

PMID:
22176987
[PubMed - indexed for MEDLINE]
5.

[Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].

Zhang YP, Wu JP, Li XT, Lei CX, Xu JZ, Yin M.

Zhonghua Fu Chan Ke Za Zhi. 2011 Sep;46(9):644-8. Chinese.

PMID:
22176986
[PubMed - indexed for MEDLINE]
6.

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.

Hillman SC, McMullan DJ, Hall G, Togneri FS, James N, Maher EJ, Meller CH, Williams D, Wapner RJ, Maher ER, Kilby MD.

Ultrasound Obstet Gynecol. 2013 Jun;41(6):610-20. doi: 10.1002/uog.12464. Epub 2013 May 7. Review.

PMID:
23512800
[PubMed - indexed for MEDLINE]
Free Article
7.

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.

Novelli A, Grati FR, Ballarati L, Bernardini L, Bizzoco D, Camurri L, Casalone R, Cardarelli L, Cavalli P, Ciccone R, Clementi M, Dalprà L, Gentile M, Gelli G, Grammatico P, Malacarne M, Nardone AM, Pecile V, Simoni G, Zuffardi O, Giardino D.

Ultrasound Obstet Gynecol. 2012 Apr;39(4):384-8. doi: 10.1002/uog.11092. Review.

PMID:
22262341
[PubMed - indexed for MEDLINE]
Free Article
8.

Chromosomal microarray versus karyotyping for prenatal diagnosis.

Wapner RJ, Martin CL, Levy B, Ballif BC, Eng CM, Zachary JM, Savage M, Platt LD, Saltzman D, Grobman WA, Klugman S, Scholl T, Simpson JL, McCall K, Aggarwal VS, Bunke B, Nahum O, Patel A, Lamb AN, Thom EA, Beaudet AL, Ledbetter DH, Shaffer LG, Jackson L.

N Engl J Med. 2012 Dec 6;367(23):2175-84. doi: 10.1056/NEJMoa1203382.

PMID:
23215555
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.

Leung TY, Vogel I, Lau TK, Chong W, Hyett JA, Petersen OB, Choy KW.

Ultrasound Obstet Gynecol. 2011 Sep;38(3):314-9. doi: 10.1002/uog.8988. Epub 2011 Aug 10.

PMID:
21400624
[PubMed - indexed for MEDLINE]
Free Article
10.

Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.

Schmid M, Stary S, Blaicher W, Gollinger M, Husslein P, Streubel B.

Prenat Diagn. 2012 Apr;32(4):376-82. doi: 10.1002/pd.2862. Epub 2011 Oct 24.

PMID:
22025351
[PubMed - indexed for MEDLINE]
11.

De novo chromosomal aberrations in the fetus; genetic counseling and clinical outcome.

Park S, Lee BY, Kim YM, Kim JM, Lee MH, Kim JW, Cho EH, Park JY, Lee YH, Yang JH, Kim MY, Han JY, Ryu HM.

J Korean Med Sci. 2003 Jun;18(3):397-401.

PMID:
12808328
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

[Results of cytogenetic examinations in fetuses with increased nuchal translucency].

Kornacki J, Ziółkowska K, Goździewicz T, Skrzypczak J.

Ginekol Pol. 2012 Mar;83(3):189-93. Polish.

PMID:
22568194
[PubMed - indexed for MEDLINE]
13.

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.

Shaffer LG, Dabell MP, Fisher AJ, Coppinger J, Bandholz AM, Ellison JW, Ravnan JB, Torchia BS, Ballif BC, Rosenfeld JA.

Prenat Diagn. 2012 Oct;32(10):976-85. doi: 10.1002/pd.3945. Epub 2012 Aug 2.

PMID:
22865506
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography.

Bellucco FT, Belangero SI, Farah LM, Machado MV, Cruz AP, Lopes LM, Lopes MA, Zugaib M, Cernach MC, Melaragno MI.

Pediatr Cardiol. 2010 Nov;31(8):1146-50. doi: 10.1007/s00246-010-9763-0. Epub 2010 Sep 17.

PMID:
20848279
[PubMed - indexed for MEDLINE]
15.

Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta-analysis.

Dhillon RK, Hillman SC, Morris RK, McMullan D, Williams D, Coomarasamy A, Kilby MD.

BJOG. 2014 Jan;121(1):11-21. doi: 10.1111/1471-0528.12382. Epub 2013 Jul 17. Review.

PMID:
23859082
[PubMed - indexed for MEDLINE]
16.

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.

Breman A, Pursley AN, Hixson P, Bi W, Ward P, Bacino CA, Shaw C, Lupski JR, Beaudet A, Patel A, Cheung SW, Van den Veyver I.

Prenat Diagn. 2012 Apr;32(4):351-61. doi: 10.1002/pd.3861. Review.

PMID:
22467166
[PubMed - indexed for MEDLINE]
17.

Ultrasonographic markers for chromosomal abnormalities in women with negative nuchal translucency and second trimester maternal serum biochemistry.

Verdin SM, Whitlow BJ, Lazanakis M, Kadir RA, Chatzipapas I, Economides DL.

Ultrasound Obstet Gynecol. 2000 Oct;16(5):402-6.

PMID:
11169322
[PubMed - indexed for MEDLINE]
Free Article
18.

An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis.

Thein AT, Abdel-Fattah SA, Kyle PM, Soothill PW.

Prenat Diagn. 2000 Apr;20(4):275-80.

PMID:
10740198
[PubMed - indexed for MEDLINE]
19.

Increased nuchal translucency thickness and normal karyotype: time for parental reassurance.

Bilardo CM, Müller MA, Pajkrt E, Clur SA, van Zalen MM, Bijlsma EK.

Ultrasound Obstet Gynecol. 2007 Jul;30(1):11-8.

PMID:
17559183
[PubMed - indexed for MEDLINE]
Free Article
20.

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.

Armengol L, Nevado J, Serra-Juhé C, Plaja A, Mediano C, García-Santiago FA, García-Aragonés M, Villa O, Mansilla E, Preciado C, Fernández L, Ángeles Mori M, García-Pérez L, Lapunzina PD, Pérez-Jurado LA.

Hum Genet. 2012 Mar;131(3):513-23. doi: 10.1007/s00439-011-1095-5.

PMID:
21975797
[PubMed - indexed for MEDLINE]
Free PMC Article

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