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Items: 1 to 20 of 154

1.

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
2.

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.

3.

Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parameters.

Bonduelle M, Van Assche E, Joris H, Keymolen K, Devroey P, Van Steirteghem A, Liebaers I.

Hum Reprod. 2002 Oct;17(10):2600-14.

5.

Microarray comparative genomic hybridization in prenatal diagnosis: a review.

Hillman SC, McMullan DJ, Williams D, Maher ER, Kilby MD.

Ultrasound Obstet Gynecol. 2012 Oct;40(4):385-91. doi: 10.1002/uog.11180. Epub 2012 Sep 17. Review.

6.

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.

7.

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
8.

Prenatal screening for and diagnosis of aneuploidy in twin pregnancies.

Audibert F, Gagnon A; 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):754-67.

PMID:
21749753
9.

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.

10.

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
11.

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.

Van den Veyver IB, Patel A, Shaw CA, Pursley AN, Kang SH, Simovich MJ, Ward PA, Darilek S, Johnson A, Neill SE, Bi W, White LD, Eng CM, Lupski JR, Cheung SW, Beaudet AL.

Prenat Diagn. 2009 Jan;29(1):29-39. doi: 10.1002/pd.2127.

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.

13.

[Clinical approach to prenatal diagnosis of chromosome abnormalities].

Herlicoviez M.

Reprod Nutr Dev. 1990;Suppl 1:139s-145s. Review. French.

PMID:
2206291
14.

Fetal and perinatal autopsy in prenatally diagnosed fetal abnormalities with normal karyotype.

Désilets V, Oligny LL; Genetics Committee of the Society of Obstetricians and Gynaecology Canada; Family Physicians Advisory Committee; Medico–Legal Committee of the SOGC.

J Obstet Gynaecol Can. 2011 Oct;33(10):1047-57. Review.

PMID:
22014783
15.

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
16.

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.

Brady PD, Delle Chiaie B, Christenhusz G, Dierickx K, Van Den Bogaert K, Menten B, Janssens S, Defoort P, Roets E, Sleurs E, Keymolen K, De Catte L, Deprest J, de Ravel T, Van Esch H, Fryns JP, Devriendt K, Vermeesch JR.

Genet Med. 2014 Jun;16(6):469-76. doi: 10.1038/gim.2013.168. Epub 2013 Oct 31.

PMID:
24177055
17.

Application of a target array comparative genomic hybridization to prenatal diagnosis.

Park JH, Woo JH, Shim SH, Yang SJ, Choi YM, Yang KS, Cha DH.

BMC Med Genet. 2010 Jun 24;11:102. doi: 10.1186/1471-2350-11-102.

18.

Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases.

Yakut S, Çetin Z, Şİmşek M, Mendilcioğlu II, Toru HS, Berker Karaüzüm S, Lüleci G.

Turk Patoloji Derg. 2015;31(1):36-44.

19.

[Data obtained by prenatal diagnosis of maternal age dependence of fetal chromosomal anomalies].

Szemere G, Faragó M, Szabó J, Hetényi M.

Orv Hetil. 1991 Dec 23;132(51):2845-9. Review. Hungarian.

PMID:
1837074
20.

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.

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