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American Journal of Occupational Therapy, ISSN 0272-9490, 11/2018, Volume 72, Issue 4_Supplement_1, p. 7211515251
This study examined age at Turner syndrome diagnosis as a factor in psychosocial difficulties. Women diagnosed after age 13 reported higher depression and more... 
Women | Medical research | Delayed | Competence | Mental health | Substance abuse | Mental depression | Medical diagnosis | Turner syndrome | Mental health care | Womens health | Health behavior | Occupational therapy | Identity | Psychosocial factors
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
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2014, Volume 211, Issue 5, pp. 527.e1 - 527.e17
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2014, Volume 111, Issue 23, pp. 8583 - 8588
Noninvasive prenatal testing using fetal DNA in maternal plasma is an actively researched area. The current generation of tests using massively parallel... 
Size distribution | Proportions | DNA | Fetus | Aneuploidy | Libraries | Sequencing | Chromosomes | Fractions | Blood plasma | Fetal aneuploidy | Next-generation sequencing | Down syndrome | Turner syndrome | Size profiling | DIGITAL PCR | CIRCULATING DNA | size profiling | fetal aneuploidy | next-generation sequencing | QUANTIFICATION | MULTIDISCIPLINARY SCIENCES | COPY NUMBER ABERRATIONS | DISTRIBUTIONS | FRACTION | FETAL CHROMOSOMAL ANEUPLOIDY | MATERNAL PLASMA | MUTATIONS | CELL-FREE DNA | Chromosomes, Human, Pair 13 - genetics | Fetal Diseases - blood | Humans | DNA - blood | Fetal Diseases - genetics | Sensitivity and Specificity | Chromosome Disorders - diagnosis | Pathology, Molecular - methods | Female | Down Syndrome - diagnosis | Electrophoresis, Capillary - methods | High-Throughput Nucleotide Sequencing - methods | Reproducibility of Results | Chromosomes, Human, X - genetics | Fetal Diseases - diagnosis | Monosomy - genetics | DNA - genetics | Monosomy - diagnosis | Pregnancy | Trisomy - diagnosis | DNA - chemistry | Trisomy - genetics | Down Syndrome - genetics | Trisomy 18 Syndrome | Trisomy 13 Syndrome | Chromosomes, Human, Pair 18 - genetics | Prenatal Diagnosis - methods | Chromosome Disorders - genetics | Genetic research | Prenatal diagnosis | Research | Nucleotide sequencing | Methods | DNA sequencing | Molecules | Plasma | Oncology | Cellular biology | Medical screening | Deoxyribonucleic acid--DNA | Index Medicus | Biological Sciences
Journal Article
Journal Article
Journal Article
Human Reproduction, ISSN 0268-1161, 10/2015, Volume 30, Issue 10, pp. 2419 - 2426
Journal Article
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 10/2006, Volume 91, Issue 10, pp. 3897 - 3902
Journal Article
Journal Article