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1. Antenatal and neonatal screening
by Leck, Ian and Wald, Nicholas J
2000, 2nd ed., ISBN 0192628267, xxii, 591
Pregnancy | Prenatal diagnosis | Newborn infants | Diagnosis | Complications | Diseases | Epidemiology | Public Health | Problems areas | Antenatal screening | Neontal screening | Technical procedures | Efficacy | Abnormality detection | Safety | Research needs
Book
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2. Prenatal diagnosis
Prenatal diagnosis, ISSN 0197-3851, 1981
Periodicals | Prenatal diagnosis
Journal
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3. Down's syndrome screening and reproductive politics
: care, choice, and disability in the prenatal clinic
by Thomas, Gareth M., author
2017, 1, Routledge studies in the sociology of health and illness, ISBN 9781138959132, xvi, 199 pages
Down syndrome | Health & Illness | Biotechnology | Qualitative Methods | Bioethics | Medicine - Sociology | Medical Ethics | Risk | Disability Studies - Sociology | Reproductive Technology Medical Sociology | Disability | Health & Medical Anthropology | Reproduction | Ethnography & Methodology | Health & Society | New Genetics | Sociology of the Family | Genetics | Sociology of Health and Illness | The Body & Identity | Medical Sociology | Social Theory | Genetic screening
Book
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4. Full Text Screening for Pre-eclampsia–Lessons from Aneuploidy Screening
by Cuckle, H.S
Placenta (Eastbourne), ISSN 0143-4004, 2010, Volume 32, Issue 1, pp. S42 - S48
Internal Medicine | Obstetrics and Gynecology | Screening | Risk | Aneuploidy | Pre-eclampsia | Markers | Life Sciences & Biomedicine | Developmental Biology | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Diagnostic Techniques, Obstetrical and Gynecological - standards | Prognosis | Genetic Testing - standards | Humans | Genetic Testing - methods | Mass Screening - methods | Pregnancy | Prenatal Diagnosis - standards | Pre-Eclampsia - blood | Sensitivity and Specificity | Female | Prenatal Diagnosis - methods | Pre-Eclampsia - diagnosis | Index Medicus
Journal Article
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5. Screening
: journal of the International Society of Neonatal Screening
International Society of Neonatal Screening
Screening, ISSN 0925-6164, 1992
Journal
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6. Full Text Genetic Screening
by Burke, Wylie and Tarini, Beth and Press, Nancy A and Evans, James P
Epidemiologic reviews, ISSN 0193-936X, 2011, Volume 33, Issue 1, pp. 148 - 164
genetics, medical | genomics | neonatal screening | heterozygote detection | prenatal diagnosis | genetic testing | Life Sciences & Biomedicine | Public, Environmental & Occupational Health | Science & Technology | Public health. Hygiene-occupational medicine | Public health. Hygiene | General aspects | Miscellaneous | Prevention and actions | Biological and medical sciences | Medical sciences | Epidemiology | Genetic Testing | Humans | Prenatal Diagnosis | Pregnancy | Mass Screening | Diagnostic Errors | Down Syndrome - genetics | Female | Primary Health Care | Down Syndrome - diagnosis | Genetic Predisposition to Disease - epidemiology | Genetic Carrier Screening | Infant, Newborn | Index Medicus
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7. Full Text Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: Clinical laboratory analysis of >72 400 specimens
by Sugarman, Elaine A and Nagan, Narasimhan and Zhu, Hui and Akmaev, Viatcheslav R and Zhou, Zhaoqing and Rohlfs, Elizabeth M and Flynn, Kerry and Hendrickson, Brant C and Scholl, Thomas and Sirko-Osadsa, Deborah Alexa and Allitto, Bernice A
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2012, Volume 20, Issue 1, pp. 27 - 32
pan-ethnic | carrier screening | SMN1 | spinal muscular atrophy (SMA) | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Neurology | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Muscular Atrophy, Spinal - diagnosis | United States - epidemiology | Humans | Male | Genetic Counseling | Genetic Testing - methods | Genetic Carrier Screening - methods | DNA Copy Number Variations | Muscular Atrophy, Spinal - genetics | Ethnic Groups - genetics | Survival of Motor Neuron 1 Protein - genetics | Adult | Female | Prenatal Diagnosis - statistics & numerical data | Reproducibility of Results | United States - ethnology | Genetic Testing - standards | Muscular Atrophy, Spinal - ethnology | Gene Frequency | Muscular Atrophy, Spinal - epidemiology | Genotype | Sequence Analysis, DNA | Fetus - cytology | Prenatal Diagnosis - standards | Mutation | Prenatal Diagnosis - methods | Laboratories | Families & family life | Cystic fibrosis | Family medical history | Minority & ethnic groups | Population genetics | Genetic screening | Hereditary diseases | Spinal muscular atrophy | Ethnicity | Prenatal diagnosis | Genetic counseling | Gene frequency | Alleles | Ethnic groups | Fibrosis | Population | Genetics | Quantitative analysis | Index Medicus
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8. REPRODUCTIVE HEALTH AND HUMAN RIGHTS: INTEGRATING MEDICINE, ETHICS, AND LAW
by COOK, REBECCA J
2003, ISSUES IN BIOMEDICAL ETHICS., ISBN 9780199241330
Moral Philosophy | Bioethics and Medical Ethics | Social and Political Philosophy | Women | Ethics | Reproductive Health | Health Care Provision | Human Rights | Medical Law | Legal Protection
Book
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9. Full Text Systematic review of first‐trimester ultrasound screening for detection of fetal structural anomalies and factors that affect screening performance
by Karim, J. N and Roberts, N. W and Salomon, L. J and Papageorghiou, A. T
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2017, Volume 50, Issue 4, pp. 429 - 441
fetal anomalies | congenital abnormalities | first trimester | prenatal diagnosis | prenatal screening | ultrasound | Acoustics | Life Sciences & Biomedicine | Technology | Radiology, Nuclear Medicine & Medical Imaging | Obstetrics & Gynecology | Science & Technology | Pregnancy | Reference Standards | Reproducibility of Results | Ultrasonography, Prenatal | Humans | Sensitivity and Specificity | Clinical Protocols | Female | Congenital Abnormalities - diagnostic imaging | Pregnancy Trimester, First | Pregnant women | Analysis | Genetic disorders | Index Medicus
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10. Full Text DNA Sequencing versus Standard Prenatal Aneuploidy Screening
by Bianchi, Diana W and Parker, R. Lamar and Wentworth, Jeffrey and Madankumar, Rajeevi and Saffer, Craig and Das, Anita F and Craig, Joseph A and Chudova, Darya I and Devers, Patricia L and Jones, Keith W and Oliver, Kelly and Rava, Richard P and Sehnert, Amy J and CARE Study Grp and CARE Study Group
The New England journal of medicine, ISSN 0028-4793, 02/2014, Volume 370, Issue 9, pp. 799 - 808
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | General aspects | Medical sciences | Chromosome aberrations | Medical genetics | Chromosomes, Human, Pair 13 - genetics | Plasma | Predictive Value of Tests | Humans | Aneuploidy | False Positive Reactions | Genetic Testing - methods | Chromosome Disorders - diagnosis | Adult | Female | Down Syndrome - diagnosis | Risk Factors | Maternal Serum Screening Tests | Pregnancy | Trisomy - diagnosis | Trisomy - genetics | Nuchal Translucency Measurement | Down Syndrome - genetics | Trisomy 18 Syndrome | Trisomy 13 Syndrome | High-Throughput Nucleotide Sequencing | Chromosomes, Human, Pair 18 - genetics | Prenatal Diagnosis - methods | Sequence Analysis, DNA - methods | Chromosome Disorders - genetics | Usage | Prenatal diagnosis | Nucleotide sequencing | Comparative analysis | Methods | DNA sequencing | Trisomy | Genetic disorders | Fetuses | Karyotypes | Prenatal development | Patau's syndrome | Medical screening | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus
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