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Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 10/2018, Volume 52, Issue S1, pp. 221 - 221
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 06/2019, Volume 39, Issue 7, pp. 571 - 572
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 12/2017, Volume 217, Issue 6, pp. 691.e1 - 691.e6
Since its debut in 2011, cell-free fetal DNA screening has undergone rapid expansion with respect to both utilization and coverage. However, conclusive data... 
amniocentesis | trisomy 13 | trisomy 21 | 47,XXY | noninvasive prenatal testing | noninvasive prenatal screening | 47,XXX | 47,XYY | cell-free DNA | NIPT | prenatal diagnosis | microdeletion syndrome | trisomy 18 | CHROMOSOMAL MICROARRAY | TRISOMIES 21 | FREE DNA | RISK | CLINICAL-EXPERIENCE | OBSTETRICS & GYNECOLOGY | FETAL ANEUPLOIDIES | Chromosome Disorders - blood | Predictive Value of Tests | Turner Syndrome - blood | Cri-du-Chat Syndrome - diagnosis | Humans | Angelman Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - genetics | Turner Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - blood | Trisomy 18 Syndrome - diagnosis | Cri-du-Chat Syndrome - genetics | Klinefelter Syndrome - blood | Klinefelter Syndrome - genetics | Sex Chromosome Aberrations | Microarray Analysis | Karyotyping | Down Syndrome - blood | Angelman Syndrome - genetics | Chorionic Villi Sampling | Chromosome Disorders - diagnosis | Prader-Willi Syndrome - genetics | Female | Down Syndrome - diagnosis | Amniocentesis | Prader-Willi Syndrome - diagnosis | Trisomy 13 Syndrome - genetics | Chromosomes, Human, X - genetics | Prader-Willi Syndrome - blood | Prenatal Diagnosis | In Situ Hybridization, Fluorescence | Cri-du-Chat Syndrome - blood | Pregnancy | Trisomy 18 Syndrome - blood | Sex Chromosome Disorders of Sex Development - diagnosis | Trisomy - diagnosis | Trisomy - genetics | Trisomy 13 Syndrome - blood | Cell-Free Nucleic Acids - blood | Trisomy 18 Syndrome - genetics | Down Syndrome - genetics | Klinefelter Syndrome - diagnosis | Turner Syndrome - genetics | Angelman Syndrome - blood | Trisomy 13 Syndrome - diagnosis | Chromosome Disorders - genetics | DNA microarrays | Medical screening | Pregnant women | Chromosomes | Analysis | Index Medicus | Abridged Index Medicus
Journal Article
2018, First edition., Human diseases and conditions collection, ISBN 1944749616, xiii, 72 pages
This book presents Down syndrome, which is the most common chromosomal disorder in humans, occurring at a rate of about 1 in 700 births. It describes the... 
Down syndrome
Book
The New England Journal of Medicine, ISSN 0028-4793, 02/2014, Volume 370, Issue 9, pp. 799 - 808
Journal Article
1985, ISBN 0039106101, xii, 435
Book
2002, ISBN 1861562306, xv, 239
This book promotes a positive message for people with Down syndrome across the world. Living with Down Syndrome is a positive experience for the majority of... 
Medical care | Patients | Down syndrome | Developmental | General | Psychology | Congresses | People with mental disabilities
Book
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2014, Volume 211, Issue 5, pp. 527.e1 - 527.e17
Journal Article
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 04/2018, Volume 51, Issue 4, pp. 470 - 479
Objectives The primary aim of this study was to compare the screening performance for trisomy 21 (T21) between combined first-trimester screening (cFTS) with... 
screening | nuchal translucency | trisomy 21 | cell‐free DNA | first‐trimester risk assessment | prenatal screening | first‐trimester screening | cell-free DNA | first-trimester screening | first-trimester risk assessment | FETAL FRACTION | METAANALYSIS | RISK | TRISOMY-21 | OBSTETRICS & GYNECOLOGY | ACOUSTICS | MATERNAL PLASMA | GESTATION | COHORT | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | BLOOD | AGE | Predictive Value of Tests | Humans | Nuchal Translucency Measurement - statistics & numerical data | Pregnancy Trimester, First | Pregnancy Outcome - epidemiology | Trisomy 18 Syndrome - diagnosis | Maternal Age | Down Syndrome - blood | Adult | Female | Down Syndrome - diagnosis | Trisomy 13 Syndrome - genetics | Risk Assessment | Down Syndrome - epidemiology | Pregnancy | Trisomy 18 Syndrome - blood | Trisomy 13 Syndrome - blood | Analysis of Variance | Cell-Free Nucleic Acids - blood | Maternal Serum Screening Tests - statistics & numerical data | Trisomy 18 Syndrome - genetics | Down Syndrome - genetics | Denmark - epidemiology | Trisomy 13 Syndrome - diagnosis | Cohort Studies | Chorionic gonadotropin | Pregnant women | DNA | Glycoproteins | Chromosomes | Blood proteins | Trisomy | Congenital diseases | Fetuses | Sex | Karyotypes | Aneuploidy | Pituitary (anterior) | Gonadotropins | Protein A | Medical screening | Blood | Prenatal care | Screening | Sensitivity | Risk assessment | Strategy | Patau's syndrome | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 09/2016, Volume 172, Issue 3, pp. 288 - 295
Journal Article
1978, [1st ed.]. --, ISBN 0521219140, xii, 366
Book
1984, ISBN 9780898851205, 371
Book
Journal Article
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