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Items: 1 to 20 of 112

1.

Antenatal screening for Down syndrome: a quantitative demonstration of the improvements over the past 20 years.

Renshaw R, Ellis K, Jacobs P, Morris J.

J Health Serv Res Policy. 2013 Oct;18(4):195-201. doi: 10.1177/1355819613482116. Epub 2013 Jul 17.

PMID:
23864125
2.

The population impact of screening for Down syndrome: audit of 19 326 invasive diagnostic tests in England and Wales in 2008.

Morris JK, Waters JJ, de Souza E.

Prenat Diagn. 2012 Jun;32(6):596-601. doi: 10.1002/pd.3866. Epub 2012 May 9.

PMID:
22573430
3.

Antenatal detection of Edwards (Trisomy 18) and Patau (Trisomy 13) syndrome: England and Wales 2005-2012.

Springett AL, Morris JK.

J Med Screen. 2014 Sep;21(3):113-9. doi: 10.1177/0969141314543128. Epub 2014 Jul 3.

PMID:
24993362
4.

Trends in timing of prenatal diagnosis and abortion for fetal chromosomal abnormalities.

Hume H, Chasen ST.

Am J Obstet Gynecol. 2015 Oct;213(4):545.e1-4. doi: 10.1016/j.ajog.2015.06.008. Epub 2015 Jun 10.

PMID:
26070711
6.

The impact of maternal serum screening on the birth prevalence of Down's syndrome and the use of amniocentesis and chorionic villus sampling in South Australia.

Cheffins T, Chan A, Haan EA, Ranieri E, Ryall RG, Keane RJ, Byron-Scott R, Scott H, Gjerde EM, Nguyen AM, Ford JH, Sykes S.

BJOG. 2000 Dec;107(12):1453-9.

7.

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
8.

Prenatal screening for Down syndrome in England and Wales and population-based birth outcomes.

Smith-Bindman R, Chu P, Bacchetti P, Waters JJ, Mutton D, Alberman E.

Am J Obstet Gynecol. 2003 Oct;189(4):980-5.

PMID:
14586339
9.

Non-invasive prenatal testing for aneuploidy: current status and future prospects.

Benn P, Cuckle H, Pergament E.

Ultrasound Obstet Gynecol. 2013 Jul;42(1):15-33. doi: 10.1002/uog.12513. Review.

10.
11.

[Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].

Wang SJ, Gao ZY, Lu YP, Li YL, You YQ, Zhang LW, Wang LX, Xu H.

Zhonghua Fu Chan Ke Za Zhi. 2012 Nov;47(11):808-12. Chinese.

PMID:
23302119
12.

[Prenatal diagnosis of chromosome aberrations after implementation of screening for Down's syndrome].

Kjaergaard S, Hahnemann JM, Skibsted L, Jensen LN, Sperling L, Zingenberg H, Kristiansen A, Brøndum-Nielsen K.

Ugeskr Laeger. 2008 Mar 31;170(14):1152-6. Danish.

PMID:
18405480
13.

The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age.

Hagen A, Entezami M, Gasiorek-Wiens A, Albig M, Becker R, Knoll U, Stumm M, Wegner RD.

Ultraschall Med. 2011 Jun;32(3):302-6. doi: 10.1055/s-0029-1245560. Epub 2010 Oct 22.

PMID:
20972947
14.

[Performance of different methods of estimating risk screening for chromosomal anomalies].

Avătăjitei MC, Moscalu M, Martiniuc V, Onofriescu M.

Rev Med Chir Soc Med Nat Iasi. 2012 Apr-Jun;116(2):515-22. Romanian.

PMID:
23077946
15.

Acceptability of serum screening as an alternative to cytogenetic diagnosis of down syndrome among women 35 years or older in Hong Kong.

Lam YH, Tang MH, Lee CP, Sin SY, Tang R, Wong HS, Wong SF.

Prenat Diagn. 2000 Jun;20(6):487-90.

PMID:
10861714
16.

Changes in the utilization of prenatal diagnosis.

Benn PA, Egan JF, Fang M, Smith-Bindman R.

Obstet Gynecol. 2004 Jun;103(6):1255-60.

PMID:
15172861
18.

Association of combined first-trimester screen and noninvasive prenatal testing on diagnostic procedures.

Larion S, Warsof SL, Romary L, Mlynarczyk M, Peleg D, Abuhamad AZ.

Obstet Gynecol. 2014 Jun;123(6):1303-10. doi: 10.1097/AOG.0000000000000275.

PMID:
24807333
19.

Access to prenatal cytogenetic diagnosis in Catania: a retrospective survey.

Agodi A, Barchitta M, Quattrocchi A, Corallo T, Venticinque V, Caruso M.

Ann Ig. 2013 Nov-Dec;25(6):529-37. doi: 10.7416/ai.2013.1953.

PMID:
24284539
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