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Advanced Search Results For "PRENATAL diagnosis"

1 - 10 of 80,567 results for
 "PRENATAL diagnosis"
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Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.

Publication Type:Academic Journal

Source(s):Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2022 Jul; Vol. 24 (7), pp. 1379-1391. Date of Electronic Publication: 2022 May 24.

Abstract:Purpose: Noninvasive prenatal screening (NIPS) using cell-free DNA has been assimilated into prenatal care. Prior studies examined clinical validity and technical performance in high-risk populations. This systematic evidence review evaluates NIPS perf...

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[Analysis of the factors influencing positive predictive value of noninvasive prenatal testing for chromosome aneuploidies].

Publication Type:Academic Journal

Source(s):Zhonghua yi xue za zhi [Zhonghua Yi Xue Za Zhi] 2022 Aug 23; Vol. 102 (31), pp. 2452-2457.

Abstract:Objective: To investigate the influence of Z -score and different risk factors on positive predictive value (PPV) of noninvasive prenatal testing (NIPT) for chromosome aneuploidies. Methods: A total of 81 838 NIPT samples from January 1, 2016 to May 31...

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Noninvasive prenatal testing suggesting an abnormality in chromosome 15 confirmed to be a case of Prader-Willi syndrome caused by trisomy rescue in the neonatal period.

Publication Type:Report

Source(s):The journal of obstetrics and gynaecology research [J Obstet Gynaecol Res] 2022 Aug; Vol. 48 (8), pp. 2214-2218. Date of Electronic Publication: 2022 Mar 23.

Abstract:We report a case of a neonatal diagnosis of Prader-Willi syndrome caused by uniparental disomy. A 34-year-old pregnant woman underwent noninvasive prenatal testing (NIPT) in a hospital that was not certified by the Japanese Association of Medical Scien...

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Performance of noninvasive prenatal screening for 22q11.2 deletion syndrome in the SMART study.

Publication Type:Report

Source(s):American journal of obstetrics and gynecology [Am J Obstet Gynecol] 2022 Jul; Vol. 227 (1), pp. 124-125. Date of Electronic Publication: 2022 Feb 02.

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Analysis of the impact of noninvasive prenatal testing for trisomies 21 and 18 in twin pregnancies undergoing artificial reproductive technology.

Publication Type:Academic Journal

Source(s):Medicine [Medicine (Baltimore)] 2022 Aug 19; Vol. 101 (33), pp. e29985.

Abstract:Purpose: The purpose of this study was to evaluate the performance and impact of noninvasive prenatal screening (NIPS) on twin pregnancies.Patients and Methods: Twin pregnancies after artificial reproductive technology(ART) were tested by NIPS for scre...

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First Trimester Noninvasive Prenatal Diagnosis of Maternally Inherited Beta-Thalassemia Mutations.

Publication Type:Editorial & Opinion

Source(s):Clinical chemistry [Clin Chem] 2022 Jul 27; Vol. 68 (8), pp. 1002-1004.

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Validation of single-gene noninvasive prenatal testing for sickle cell disease.

Publication Type:Report

Source(s):American journal of hematology [Am J Hematol] 2022 Jul; Vol. 97 (7), pp. E270-E273. Date of Electronic Publication: 2022 May 02.

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Audit of the first > 7500 noninvasive prenatal aneuploidy tests in a Swiss genetics center.

Publication Type:Academic Journal

Source(s):Archives of gynecology and obstetrics [Arch Gynecol Obstet] 2022 May; Vol. 305 (5), pp. 1185-1192. Date of Electronic Publication: 2021 Sep 17.

Abstract:Objectives: Noninvasive prenatal testing (NIPT) is actually the most accurate method of screening for fetal chromosomal aberration (FCA). We used pregnancy outcome record to evaluate a complete data set of single nucleotide polymorphism-based test resu...

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Evaluating Expanded Noninvasive Prenatal Screening.

Publication Type:Academic Journal

Source(s):Obstetrics and gynecology [Obstet Gynecol] 2022 Jun 01; Vol. 139 (6), pp. 1009-1011. Date of Electronic Publication: 2022 May 02.

Abstract:Public attention has been drawn recently to the commercial availability of noninvasive prenatal screening for rare genetic conditions, despite estimates that the positive predictive value of such tests is low. Many have focused on the importance of edu...

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Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening.

Publication Type:Academic Journal

Source(s):Obstetrics and gynecology [Obstet Gynecol] 2022 May 01; Vol. 139 (5), pp. 877-887. Date of Electronic Publication: 2022 Apr 05.

Abstract:Objective: To examine the effect of maternal age on the rate of clinically significant chromosomal microarray analysis results in pregnancies with abnormal maternal serum screening and to establish the residual risk for abnormal microarray findings aft...

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