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1. Human prenatal diagnosis
by Filkins, Karen and Russo, Joseph F
1985, ISBN 9780824773687, Volume 18., xv, 418
Prenatal diagnosis
Book
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2. Human prenatal diagnosis
by Filkins, Karen, 1946 and Russo, Joseph F., 1945
1990, 2nd ed., rev. and expanded. --, ISBN 082478314X, xvii, 601
Prenatal Diagnosis | methods
Book
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3. Full Text Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
by Wapner, Ronald J and Martin, Christa Lese and Levy, Brynn and Ballif, Blake C and Eng, Christine M and Zachary, Julia M and Savage, Melissa and Platt, Lawrence D and Saltzman, Daniel and Grobman, William A and Klugman, Susan and Scholl, Thomas and Simpson, Joe Leigh and McCall, Kimberly and Aggarwal, Vimla S and Bunke, Brian and Nahum, Odelia and Patel, Ankita and Lamb, Allen N and Thom, Elizabeth A and Beaudet, Arthur L and Ledbetter, David H and Shaffer, Lisa G and Jackson, Laird
The New England Journal of Medicine, ISSN 0028-4793, 12/2012, Volume 367, Issue 23, pp. 2175 - 2184
This large, systematic study of prenatal diagnosis shows that chromosomal microarray analysis provided additional, clinically significant cytogenetic... 
MEDICINE, GENERAL & INTERNAL | COPY-NUMBER VARIANTS | DOWN-SYNDROME | DEVELOPMENTAL-DISABILITIES | COMPARATIVE GENOMIC HYBRIDIZATION | CONGENITAL-ANOMALIES | IDENTIFICATION | REARRANGEMENTS | SNP ARRAY | CLINICAL-SIGNIFICANCE | ARRAY ANALYSIS | Fetal Diseases - diagnosis | Oligonucleotide Array Sequence Analysis | Chromosomes, Human - genetics | Humans | Genetic Testing - methods | Pregnancy | Maternal Age | Ultrasonography, Prenatal | Karyotyping | Chromosome Aberrations | Chromosome Disorders - diagnosis | Adult | Female | Down Syndrome - diagnosis | Prenatal Diagnosis - methods | Karyotype | Usage | DNA microarrays | Prenatal diagnosis | Diagnosis | Research | Comparative analysis | Developmental delay | Health aspects | Methods | Fetuses | Genes | Tissue culture | Prenatal development | Genomes | Medical diagnosis | Autism | Chromosome translocations | Down's syndrome | Ultrasonography | Children | Triploidy | Chromosomes | Index Medicus | Abridged Index Medicus
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4. Prenatal diagnosis
2006, ISBN 9780838576823, xxi, 767
Book
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5. Fetology
: diagnosis and management of the fetal patient
by Bianchi, Diana W
2010, 2nd ed., OBGYN Collection, ISBN 9780071442015, xix, 1004
"This book was written to provide a multidisciplinary approach to the full implications of a fetal sonographic or chromosomal diagnosis--from prenatal... 
Prenatal Diagnosis | therapy | methods | Fetal Diseases | Perinatal Care | diagnosis | Fetal Monitoring | Fetus
Book
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6. Full Text ESC Guidelines on the management of cardiovascular diseases during pregnancy: the Task Force on the Management of Cardiovascular Diseases during Pregnancy of the European Society of Cardiology (ESC)
by Regitz-Zagrosek, Vera and Blomstrom Lundqvist, Carina and Borghi, Claudio and Cifkova, Renata and Ferreira, Rafael and Foidart, Jean-Michel and Gibbs, J. Simon R and Gohlke-Baerwolf, Christa and Gorenek, Bulent and Iung, Bernard and Kirby, Mike and Maas, Angela H. E. M and Morais, Joao and Nihoyannopoulos, Petros and Pieper, Petronella G and Presbitero, Patrizia and Roos-Hesselink, Jolien W and Schaufelberger, Maria and Seeland, Ute and Torracca, Lucia and Bax, Jeroen and Auricchio, Angelo and Baumgartner, Helmut and Ceconi, Claudio and Dean, Veronica and Deaton, Christi and Fagard, Robert and Funck-Brentano, Christian and Hasdai, David and Hoes, Arno and Knuuti, Juhani and Kolh, Philippe and McDonagh, Theresa and Moulin, Cyril and Poldermans, Don and Popescu, Bogdan A and Reiner, Zeljko and Sechtem, Udo and Sirnes, Per Anton and Torbicki, Adam and Vahanian, Alec and Windecker, Stephan and Aguiar, Carlos and Al-Attar, Nawwar and Garcia, Angeles Alonso and Antoniou, Anna and Coman, Ioan and Elkayam, Uri and Gomez-Sanchez, Miguel Angel and Gotcheva, Nina and Hilfiker-Kleiner, Denise and Kiss, Robert Gabor and Kitsiou, Anastasia and Konings, Karen T. S and Lip, Gregory Y. H and Manolis, Athanasios and Mebaaza, Alexane and Mintale, Iveta and Morice, Marie-Claude and Mulder, Barbara J and Pasquet, Agnès and Price, Susanna and Priori, Silvia G and Salvador, Maria J and Shotan, Avraham and Silversides, Candice K and Skouby, Sven O and Stein, Jörg-Ingolf and Tornos, Pilar and Vejlstrup, Niels and Walker, Fiona and Warnes, Carole and Task Force and ESC Comm Practice Guidelines CPG and European Society of Gynecology (ESG) and Association for European Paediatric Cardiology (AEPC) and German Society for Gender Medicine (DGesGM) and ESC Committee for Practice Guidelines and Endorsed by the European Society of Gynecology (ESG), the Association for European Paediatric Cardiology (AEPC), and the German Society for Gender Medicine (DGesGM) and ESC Committee for Practice Guidelines (CPG) and Authors/Task Force Members and Document Reviewers and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper
European heart journal, ISSN 0195-668X, 2011, Volume 32, Issue 24, pp. 3147 - 3197
Hypertension | Heart failure | PERIPARTUM CARDIOMYOPATHY | CARDIAC & CARDIOVASCULAR SYSTEMS | Arrhythmia | VENOUS THROMBOEMBOLIC DISEASE | Cardiovascular disease | Management | Guidelines | ATRIAL-FIBRILLATION | Pregnancy | Valvular heart disease | ACC/AHA/ESC 2006 GUIDELINES | Congential heart disease | Risk assessment | CONGENITAL HEART-DISEASE | MOLECULAR-WEIGHT HEPARIN | PULMONARY-EMBOLISM | ACUTE MYOCARDIAL-INFARCTION | BICUSPID AORTIC-VALVE | EHLERS-DANLOS-SYNDROME | Pregnancy Complications, Cardiovascular - therapy | Prenatal Care - methods | Humans | Aortic Diseases - therapy | Abortion, Induced - methods | Aortic Diseases - diagnosis | Contraindications | Heart Diseases - diagnosis | Cardiovascular Agents - therapeutic use | Heart Diseases - therapy | Counseling - methods | Female | Hypertension - therapy | Pregnancy Complications, Cardiovascular - diagnosis | Hypertension - diagnosis | Prenatal Diagnosis - methods | Pregnancy Complications, Infectious - therapy | Venous Thromboembolism - therapy | Pregnancy Complications, Infectious - diagnosis | Venous Thromboembolism - diagnosis | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap
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7. Prenatal diagnosis in obstetric practice
by Connor, J. M. 1951- (James Michael) and Whittle, Martin J
1989, ISBN 063201945X, xi, 274
Prenatal diagnosis
Book
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8. Fetal medicine
: prenatal diagnosis and management
by Boué, André and Boué, A
1995, Oxford medical publications., ISBN 0192619047, Volume no. 26., xi, 292
Fetus | Prenatal diagnosis | Abnormalities | Diseases
Book
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9. Full Text Noninvasive Prenatal Diagnosis of Fetal Chromosomal Aneuploidy by Massively Parallel Genomic Sequencing of DNA in Maternal Plasma
by Rossa W. K. Chiu and K. C. Allen Chan and Yuan Gao and Virginia Y. M. Lau and Wenli Zheng and Tak Y. Leung and Chris H. F. Foo and Bin Xie and Nancy B. Y. Tsui and Fiona M. F. Lun and Benny C. Y. Zee and Tze K. Lau and Charles R. Cantor and Y. M. Dennis Lo
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2008, Volume 105, Issue 51, pp. 20458 - 20463
Chromosomal aneuploidy is the major reason why couples opt for prenatal diagnosis. Current methods for definitive diagnosis rely on invasive procedures, such... 
Sex chromosomes | Molecules | Prenatal diagnosis | DNA | Genomics | Fetus | Aneuploidy | Chromosomes | Sequencing | Blood plasma | Trisomy 21 | Solexa sequencing | Down syndrome | AMNIOCENTESIS | DIGITAL PCR | CELLS | trisomy 21 | MULTIDISCIPLINARY SCIENCES | SERUM | TRISOMY-21 | WOMEN | MESSENGER-RNA | PLACENTAL ORIGIN | BLOOD | DNA - genetics | Pregnancy | Humans | Female | Genomics - methods | Prenatal Diagnosis - methods | Mothers | Sequence Analysis, DNA | DNA - blood | Infants (Newborn) | Usage | Diagnosis | Nucleotide sequencing | Methods | Diseases | Plasma | Prenatal development | Gene loci | Medical diagnosis | Deoxyribonucleic acid--DNA | Amniocentesis | Trisomy | Nucleotide sequence | Fetuses | Genomes | Villus | Abortion | Polymerase chain reaction | Counting methods | genomics | Sampling | DNA sequencing | Index Medicus | Biological Sciences
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10. 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, ISSN 1018-4813, 01/2012, Volume 20, Issue 1, pp. 27 - 32
Spinal muscular atrophy (SMA) is a leading inherited cause of infant death with a reported incidence of similar to 1 in 10 000 live births and is second to... 
pan-ethnic | carrier screening | SMN1 | spinal muscular atrophy (SMA) | COPIES | DEPENDENT PROBE AMPLIFICATION | SMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHENOTYPE | IDENTIFICATION | QUANTITATIVE-ANALYSIS | COPY NUMBER | GENETICS & HEREDITY | 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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11. 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
Sequencing of fetal DNA in maternal blood to detect trisomies had a significantly lower false positive rate than the standard method of biochemical assay and... 
POPULATION | MEDICINE, GENERAL & INTERNAL | 1ST-TRIMESTER | TRISOMIES 21 | MATERNAL PLASMA | CONFINED PLACENTAL MOSAICISM | EXPERIENCE | TRISOMY-21 | FREE FETAL DNA | CELL-FREE DNA | BLOOD | 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 | Risk groups | Fetuses | Karyotypes | Prenatal development | Patau's syndrome | Medical screening | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus
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12. Essentials of prenatal diagnosis
by Elias, Sherman and Simpson, Joe Leigh, 1943
1993, ISBN 9780443087806, xv, 431
Fetal Diseases | diagnosis | Prenatal Diagnosis | therapy | methods
Book
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13. Atlas of preimplantation genetic diagnosis
by Verlinsky, Yury and Kuliev, Anver
2005, 2nd ed., ISBN 1842142453, xiv, 288
Genetic Diseases, Inborn | Preimplantation genetic diagnosis | prevention & control | Prenatal Diagnosis | methods | Preimplantation Diagnosis
Book
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14. Full Text Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing
by Stephanie C. Y. Yu and K. C. Allen Chan and Yama W. L. Zheng and Peiyong Jiang and Gary J. W. Liao and Hao Sun and Ranjit Akolekar and Tak Y. Leung and Attie T. J. I. Go and John M. G. van Vugt and Ryoko Minekawa and Cees B. M. Oudejans and Kypros H. Nicolaides and Rossa W. K. Chiu and Y. M. Dennis Lo
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
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15.