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Results: 1 to 20 of 100

1.

Referral patterns for microarray testing in prenatal diagnosis.

Shaffer LG, Dabell MP, Rosenfeld JA, Neill NJ, Ballif BC, Coppinger J, Diwan NR, Chong K, Shohat M, Chitayat D.

Prenat Diagn. 2012 Apr;32(4):344-50. doi: 10.1002/pd.3856. Erratum in: Prenat Diagn. 2012 Jun;32(6):611.

PMID:
22467165
[PubMed - indexed for MEDLINE]
2.

Prenatal screening for fetal aneuploidy in singleton pregnancies.

Chitayat D, Langlois S, Wilson RD; Genetics Committee of the Society of Obstetricians and Gynaecologists of Canada; Prenatal Diagnosis Committee of the Canadian College of Medical Geneticists.

J Obstet Gynaecol Can. 2011 Jul;33(7):736-50.

PMID:
21749752
[PubMed - indexed for MEDLINE]
3.

Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray.

Coppinger J, Alliman S, Lamb AN, Torchia BS, Bejjani BA, Shaffer LG.

Prenat Diagn. 2009 Dec;29(12):1156-66. doi: 10.1002/pd.2371.

PMID:
19795450
[PubMed - indexed for MEDLINE]
4.

The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testing.

Ogilvie CM, Lashwood A, Chitty L, Waters JJ, Scriven PN, Flinter F.

BJOG. 2005 Oct;112(10):1369-75.

PMID:
16167939
[PubMed - indexed for MEDLINE]
5.

Referral patterns for microarray testing in prenatal diagnosis.

Shaffer LG, Dabell MP, Rosenfeld JA, Neill NJ, Ballif BC, Coppinger J, Diwan NR, Chong K, Shohat M, Chitayat D.

Prenat Diagn. 2012 Jun;32(6):611. doi: 10.1002/pd.3909. No abstract available.

PMID:
22622835
[PubMed - indexed for MEDLINE]
6.

Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.

Langlois S, Duncan A.

J Obstet Gynaecol Can. 2011 Sep;33(9):955-60. Review.

PMID:
21923994
[PubMed - indexed for MEDLINE]
7.

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]
8.

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]
9.

Comparative genomic hybridization and prenatal diagnosis.

Van den Veyver IB, Beaudet AL.

Curr Opin Obstet Gynecol. 2006 Apr;18(2):185-91. Review.

PMID:
16601480
[PubMed - indexed for MEDLINE]
10.

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.

Hillman SC, Pretlove S, Coomarasamy A, McMullan DJ, Davison EV, Maher ER, Kilby MD.

Ultrasound Obstet Gynecol. 2011 Jan;37(1):6-14. doi: 10.1002/uog.7754. Review.

PMID:
20658510
[PubMed - indexed for MEDLINE]
Free Article
11.

Prenatal diagnosis using array CGH.

Kashork CD, Theisen A, Shaffer LG.

Methods Mol Biol. 2008;444:59-69. doi: 10.1007/978-1-59745-066-9_5.

PMID:
18425472
[PubMed - indexed for MEDLINE]
12.

Prenatal diagnosis using array-CGH: a French experience.

Rooryck C, Toutain J, Cailley D, Bouron J, Horovitz J, Lacombe D, Arveiler B, Saura R.

Eur J Med Genet. 2013 Jul;56(7):341-5. doi: 10.1016/j.ejmg.2013.02.003. Epub 2013 Feb 20.

PMID:
23454632
[PubMed - indexed for MEDLINE]
13.

0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practice.

Srebniak MI, Mout L, Van Opstal D, Galjaard RJ.

Hum Mutat. 2013 Sep;34(9):1298-303. doi: 10.1002/humu.22355. Epub 2013 Jun 6.

PMID:
23674485
[PubMed - indexed for MEDLINE]
14.

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.

Shaffer LG, Coppinger J, Alliman S, Torchia BA, Theisen A, Ballif BC, Bejjani BA.

Prenat Diagn. 2008 Sep;28(9):789-95. doi: 10.1002/pd.2053.

PMID:
18646242
[PubMed - indexed for MEDLINE]
15.

Genomic microarrays: a technology overview.

Brady PD, Vermeesch JR.

Prenat Diagn. 2012 Apr;32(4):336-43. doi: 10.1002/pd.2933. Review.

PMID:
22467164
[PubMed - indexed for MEDLINE]
16.

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

Rickman L, Fiegler H, Shaw-Smith C, Nash R, Cirigliano V, Voglino G, Ng BL, Scott C, Whittaker J, Adinolfi M, Carter NP, Bobrow M.

J Med Genet. 2006 Apr;43(4):353-61. Epub 2005 Sep 30.

PMID:
16199537
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Evaluation of prenatally diagnosed structural congenital anomalies.

Gagnon A, Wilson RD, Allen VM, Audibert F, Blight C, Brock JA, Désilets VA, Johnson JA, Langlois S, Murphy-Kaulbeck L, Wyatt P; Society of Obstetricians and Gynaecologists of Canada.

J Obstet Gynaecol Can. 2009 Sep;31(9):875-81, 882-9. Review. English, French.

PMID:
19941713
[PubMed - indexed for MEDLINE]
18.

Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial.

Wapner RJ, Driscoll DA, Simpson JL.

Prenat Diagn. 2012 Apr;32(4):396-400. doi: 10.1002/pd.3863.

PMID:
22467170
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

From karyotyping to array-CGH in prenatal diagnosis.

Lichtenbelt KD, Knoers NV, Schuring-Blom GH.

Cytogenet Genome Res. 2011;135(3-4):241-50. doi: 10.1159/000334065. Epub 2011 Nov 12. Review.

PMID:
22086062
[PubMed - indexed for MEDLINE]
20.

Prenatal cytogenetic diagnosis in Spain: analysis and evaluation of the results obtained from amniotic fluid samples during the last decade.

Mademont-Soler I, Morales C, Clusellas N, Soler A, Sánchez A; Group of Cytogenetics from Hospital Clínic de Barcelona.

Eur J Obstet Gynecol Reprod Biol. 2011 Aug;157(2):156-60. doi: 10.1016/j.ejogrb.2011.03.016. Epub 2011 Apr 13.

PMID:
21492994
[PubMed - indexed for MEDLINE]

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