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Items: 1 to 20 of 108

1.

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.

2.

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.

McGillivray G, Rosenfeld JA, McKinlay Gardner RJ, Gillam LH.

Prenat Diagn. 2012 Apr;32(4):389-95. doi: 10.1002/pd.3849.

PMID:
22467169
3.

Developing standards for chromosomal microarray testing counselling in paediatrics.

Godfrey E, Clark P.

Acta Paediatr. 2014 Jun;103(6):574-7. doi: 10.1111/apa.12601. Epub 2014 Mar 17.

PMID:
24528481
4.

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.

5.

Chromosome microarrays in human reproduction.

Rajcan-Separovic E.

Hum Reprod Update. 2012 Sep-Oct;18(5):555-67. doi: 10.1093/humupd/dms023. Epub 2012 Jun 2. Review.

PMID:
22661549
6.

Ethical controversies in prenatal microarray.

Stark Z, Gillam L, Walker SP, McGillivray G.

Curr Opin Obstet Gynecol. 2013 Apr;25(2):133-7. doi: 10.1097/GCO.0b013e32835ebb67. Review.

PMID:
23454982
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
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.

9.

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.

Bernhardt BA, Kellom K, Barbarese A, Faucett WA, Wapner RJ.

J Genet Couns. 2014 Dec;23(6):938-47. doi: 10.1007/s10897-014-9702-y. Epub 2014 Feb 27.

10.

Chromosomal microarray analysis and prenatal diagnosis.

Lo JO, Shaffer BL, Feist CD, Caughey AB.

Obstet Gynecol Surv. 2014 Oct;69(10):613-21. doi: 10.1097/OGX.0000000000000119. Review.

PMID:
25336071
11.

Evolving applications of microarray analysis in prenatal diagnosis.

Savage MS, Mourad MJ, Wapner RJ.

Curr Opin Obstet Gynecol. 2011 Apr;23(2):103-8. doi: 10.1097/GCO.0b013e32834457c7. Review.

12.

Eunice Kennedy Shriver National Institute of Child Health and Human Development Pediatric Formulation Initiative: selected reports from working groups.

Giacoia GP, Taylor-Zapata P, Mattison D.

Clin Ther. 2008 Nov;30(11):2097-101. doi: 10.1016/j.clinthera.2008.11.017.

PMID:
19108797
13.

Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis.

American College of Obstetricians and Gynecologists Committee on Genetics.

Obstet Gynecol. 2013 Dec;122(6):1374-7. doi: 10.1097/01.AOG.0000438962.16108.d1.

PMID:
24264715
14.

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
15.

Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.

Pan M, Han J, Zhen L, Yang X, Li R, Liao C, Li DZ.

Eur J Obstet Gynecol Reprod Biol. 2016 Feb;197:164-7. doi: 10.1016/j.ejogrb.2015.12.024. Epub 2015 Dec 30.

PMID:
26771907
16.

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.

17.

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.

18.

Karyotype versus microarray testing for genetic abnormalities after stillbirth.

Reddy UM, Page GP, Saade GR, Silver RM, Thorsten VR, Parker CB, Pinar H, Willinger M, Stoll BJ, Heim-Hall J, Varner MW, Goldenberg RL, Bukowski R, Wapner RJ, Drews-Botsch CD, O'Brien BM, Dudley DJ, Levy B; NICHD Stillbirth Collaborative Research Network.

N Engl J Med. 2012 Dec 6;367(23):2185-93. doi: 10.1056/NEJMoa1201569.

19.

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
20.

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

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