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Items: 1 to 20 of 99

1.

Clinical utility of chromosomal microarray analysis in prenatal diagnosis: report of first 6 months in clinical practice.

Klugman S, Suskin B, Spencer BL, Dar P, Bajaj K, Powers J, Reichling J, Wasserman D, Dolan SM, Merkatz IR.

J Matern Fetal Neonatal Med. 2014 Sep;27(13):1333-8. doi: 10.3109/14767058.2013.858243. Epub 2013 Nov 26.

PMID:
24147763
2.

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
3.

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.

4.

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.

5.

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
6.

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
7.

Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?

Ganesamoorthy D, Bruno DL, McGillivray G, Norris F, White SM, Adroub S, Amor DJ, Yeung A, Oertel R, Pertile MD, Ngo C, Arvaj AR, Walker S, Charan P, Palma-Dias R, Woodrow N, Slater HR.

BJOG. 2013 Apr;120(5):594-606. doi: 10.1111/1471-0528.12150. Epub 2013 Jan 18.

8.

[Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].

Wu X, Fu F, Li R, Pan M, Han J, Zhen L, Yang X, Zhang Y, Li F, Liao C.

Zhonghua Fu Chan Ke Za Zhi. 2014 Dec;49(12):893-8. Chinese.

PMID:
25608988
9.

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
10.

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.

11.

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
12.

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.

Lu X, Shaw CA, Patel A, Li J, Cooper ML, Wells WR, Sullivan CM, Sahoo T, Yatsenko SA, Bacino CA, Stankiewicz P, Ou Z, Chinault AC, Beaudet AL, Lupski JR, Cheung SW, Ward PA.

PLoS One. 2007 Mar 28;2(3):e327.

13.

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.

14.

Dilemmas in Genetic Counseling for Low-Penetrance Neuro-Susceptibility Loci Detected on Prenatal Chromosomal Microarray Analysis.

Brabbing-Goldstein D, Reches A, Svirsky R, Bar-Shira A, Yaron Y.

Am J Obstet Gynecol. 2017 Nov 13. pii: S0002-9378(17)32324-4. doi: 10.1016/j.ajog.2017.11.559. [Epub ahead of print]

PMID:
29146387
15.

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.

Lee CN, Lin SY, Lin CH, Shih JC, Lin TH, Su YN.

BJOG. 2012 Apr;119(5):614-25. doi: 10.1111/j.1471-0528.2012.03279.x. Epub 2012 Feb 7.

16.

Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes.

Mikhaelian M, Veach PM, MacFarlane I, LeRoy BS, Bower M.

Prenat Diagn. 2013 Apr;33(4):371-7. doi: 10.1002/pd.4071. Epub 2013 Mar 1.

PMID:
23450520
17.

Chromosomal microarray use among women undergoing invasive prenatal diagnosis.

Naqvi M, Goldfarb IT, Hanmer KJ, Bryant A.

Prenat Diagn. 2016 Jul;36(7):656-61. doi: 10.1002/pd.4835. Epub 2016 Jun 9.

PMID:
27130707
18.

[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
19.

Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies.

Li R, Fu F, Zhang YL, Li DZ, Liao C.

Taiwan J Obstet Gynecol. 2014 Dec;53(4):579-82. doi: 10.1016/j.tjog.2014.05.004.

20.

[Study on key techniques and intervention in reducing birth defects].

Zhu BS, Su J, Lu XH, He J, Zhu S, Jiao CX, Zhang JM, Tang XH, Tao Y, Lin KP, Chen H, Li SY.

Zhonghua Fu Chan Ke Za Zhi. 2011 Sep;46(9):658-63. Chinese.

PMID:
22176989

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