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Results: 1 to 20 of 29

1.

BACs-on-Beads technology: a reliable test for rapid detection of aneuploidies and microdeletions in prenatal diagnosis.

García-Herrero S, Campos-Galindo I, Martínez-Conejero JA, Serra V, Olmo I, Lara C, Simón C, Rubio C.

Biomed Res Int. 2014;2014:590298. doi: 10.1155/2014/590298. Epub 2014 Mar 27.

PMID:
24795887
[PubMed - in process]
Free PMC Article
2.

Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.

Manolakos E, Kefalas K, Vetro A, Oikonomidou E, Daskalakis G, Psara N, Siomou E, Papageorgiou E, Sevastopoulou E, Konstantinidou A, Vrachnis N, Thomaidis L, Zuffardi O, Papoulidis I.

Mol Cytogenet. 2013 Oct 31;6(1):47. doi: 10.1186/1755-8166-6-47.

PMID:
24176130
[PubMed]
Free PMC Article
3.

The 'thousand-dollar genome': an ethical exploration.

Dondorp WJ, de Wert GM.

Eur J Hum Genet. 2013 Jun;21 Suppl 1:S6-26. doi: 10.1038/ejhg.2013.73.

PMID:
23677179
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

An improved method to extract DNA from 1 ml of uncultured amniotic fluid from patients at less than 16 weeks' gestation.

Mosca-Boidron AL, Faivre L, Aho S, Marle N, Truntzer C, Rousseau T, Ragon C, Payet M, Thauvin-Robinet C, Thevenon J, El Chehadeh S, Huet F, Sagot P, Mugneret F, Callier P.

PLoS One. 2013;8(4):e59956. doi: 10.1371/journal.pone.0059956. Epub 2013 Apr 2.

PMID:
23565177
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.

Evangelidou P, Alexandrou A, Moutafi M, Ioannides M, Antoniou P, Koumbaris G, Kallikas I, Velissariou V, Sismani C, Patsalis PC.

Biomed Res Int. 2013;2013:346762. doi: 10.1155/2013/346762. Epub 2013 Mar 4. Review.

PMID:
23555083
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

The utility of chromosomal microarray analysis in developmental and behavioral pediatrics.

Beaudet AL.

Child Dev. 2013 Jan-Feb;84(1):121-32. doi: 10.1111/cdev.12050. Epub 2013 Jan 11.

PMID:
23311723
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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
9.

The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.

de Jong A, Dondorp WJ, Krumeich A, Boonekamp J, van Lith JM, de Wert GM.

J Community Genet. 2013 Jan;4(1):125-35. doi: 10.1007/s12687-012-0126-9. Epub 2012 Nov 9.

PMID:
23138342
[PubMed]
Free PMC Article
10.

Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns.

Coughlin CR 2nd, Scharer GH, Shaikh TH.

Genome Med. 2012 Oct 30;4(10):80. doi: 10.1186/gm381. eCollection 2012. Review.

PMID:
23114084
[PubMed]
Free PMC Article
11.

Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies.

Filges I, Kang A, Klug V, Wenzel F, Heinimann K, Tercanli S, Miny P.

Mol Cytogenet. 2012 Sep 17;5(1):38. doi: 10.1186/1755-8166-5-38.

PMID:
22979998
[PubMed]
Free PMC Article
12.

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.

Bernhardt BA, Soucier D, Hanson K, Savage MS, Jackson L, Wapner RJ.

Genet Med. 2013 Feb;15(2):139-45. doi: 10.1038/gim.2012.113. Epub 2012 Sep 6.

PMID:
22955112
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.

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

Prenat Diagn. 2012 Oct;32(10):986-95. doi: 10.1002/pd.3943. Epub 2012 Jul 30.

PMID:
22847778
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Now you can! Reality & Future Applications of array CGH in prenatal diagnosis.

Postorivo D, Nardone AM, Biancolella M, Mesoraca A, Novelli G.

J Prenat Med. 2009 Apr;3(2):23-4. No abstract available.

PMID:
22439036
[PubMed]
Free PMC Article
16.

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.

Srebniak MI, Boter M, Oudesluijs GO, Cohen-Overbeek T, Govaerts LC, Diderich KE, Oegema R, Knapen MF, van de Laar IM, Joosten M, Van Opstal D, Galjaard RJ.

Mol Cytogenet. 2012 Mar 13;5(1):14. doi: 10.1186/1755-8166-5-14.

PMID:
22413963
[PubMed]
Free PMC Article
17.

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
18.

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths.

Harris RA, Ferrari F, Ben-Shachar S, Wang X, Saade G, Van Den Veyver I, Facchinetti F, Aagaard-Tillery K.

Prenat Diagn. 2011 Oct;31(10):932-44. doi: 10.1002/pd.2817. Epub 2011 Jul 5.

PMID:
21732394
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Genetic screening.

Burke W, Tarini B, Press NA, Evans JP.

Epidemiol Rev. 2011 Jul;33(1):148-64. doi: 10.1093/epirev/mxr008. Epub 2011 Jun 27. Review.

PMID:
21709145
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.

Srebniak M, Boter M, Oudesluijs G, Joosten M, Govaerts L, Van Opstal D, Galjaard RJ.

Eur J Hum Genet. 2011 Dec;19(12):1230-7. doi: 10.1038/ejhg.2011.119. Epub 2011 Jun 22.

PMID:
21694736
[PubMed - indexed for MEDLINE]
Free PMC Article

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