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2015, Clinics in developmental medicine (unnumbered), ISBN 9781909962477, xvii, 296
Book
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
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
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 1/2018, Volume 48, Issue 1, pp. 326 - 331
Journal Article
2012, 1st ed., Progress in brain research, ISBN 9780444542991, Volume 197., x, 262
Down syndrome (DS) is the most common example of neurogenetic aneuploid disorder leading to mental retardation. In most cases, DS results from an extra copy of... 
Developmental neurobiology | Down syndrome
Book
1997, 2nd ed., Oxford medical publications., ISBN 0192626620, xii, 192
Book
2012, 1st ed., Progress in brain research, ISBN 044454299X, Volume 197.
Web Resource
1964, A publication from the Institute for Medical Genetics of the University of Uppsala, Sweden, 196
Book
1972, Studies in social and economic process, 131
Book
2011, ISBN 9781107400436, xiii, 237
Down syndrome is one of the most commonly occurring developmental disorders and it is now possible to conceptualize and define opportunities for neurocognitive... 
Children with disabilities | Preschool children | Identification | Down syndrome | Rehabilitation | Learning disabled children | Patients
Book
2017, Routledge studies in the sociology of health and illness, ISBN 9781138959132, xvi, 199 pages
In the UK and beyond, Down’s syndrome screening has become a universal programme in prenatal care. But why does screening persist, particularly in light of... 
Down syndrome | Health & Society | Diagnostic Tests, Routine - ethics | Genetic screening
Book
Nature Genetics, ISSN 1061-4036, 11/2009, Volume 41, Issue 11, pp. 1243 - 1246
Journal Article
1995, ISBN 052146532X, xiii, 202
The most common, most easily recognised and probably the most researched single condition causing learning disability - Down's syndrome. Based on extensive... 
Patients | Longitudinal studies | Down syndrome
Book
03/2016, Resource Materials for Children Ser., ISBN 113814309X
Annotation This practical handbook offers advice on strategies for meeting the special educational needs of children with Down's syndrome in mainstream... 
Down Syndrome | Medical
Web Resource