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The Pediatric clinics of North America, ISSN 0031-3955, 2015, Volume 62, Issue 2, pp. 411 - 426
Journal Article
American journal of obstetrics and gynecology, ISSN 0002-9378, 12/2017, Volume 217, Issue 6, pp. 691.e1 - 691.e6
... recently added chromosomal microdeletion syndromes, have lagged behind. Thus, there is a continued need to educate clinicians and patients about the current benefits... 
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 | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | 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... 
Down syndrome
Book
Journal of autism and developmental disorders, ISSN 1573-3432, 10/2017, Volume 48, Issue 1, pp. 326 - 331
Journal Article
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 05/2014, Volume 111, Issue 23, pp. 8583 - 8588
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2016, Volume 65, pp. 1 - 13
Journal Article
The New England journal of medicine, ISSN 1533-4406, 02/2014, Volume 370, Issue 9, pp. 799 - 808
Journal Article
Clinics in laboratory medicine, ISSN 0272-2712, 06/2012, Volume 32, Issue 2, pp. 231 - 248
Down syndrome is the most common genetic cause of mental retardation. Its frequency at birth in a population varies with maternal age distribution at birth... 
Folate metabolism | Down syndrome | Noninvasive prenatal diagnosis | Cytogenetic studies | Screening and prenatal diagnosis | Future therapies | Life Sciences & Biomedicine | Medical Laboratory Technology | Science & Technology | Pregnancy | Animals | Humans | Female | Mice | Cytogenetic Analysis | Down Syndrome - diagnosis | Prenatal Diagnosis - methods
Journal Article