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1985, ISBN 9780824773687, Volume 18., xv, 418
Book
1990, 2nd ed., rev. and expanded. --, ISBN 082478314X, xvii, 601
Book
The New England Journal of Medicine, ISSN 0028-4793, 12/2012, Volume 367, Issue 23, pp. 2175 - 2184
Journal Article
2006, ISBN 9780838576823, xxi, 767
Book
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
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
Journal Article
1995, Oxford medical publications., ISBN 0192619047, Volume no. 26., xi, 292
Book
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2012, Volume 20, Issue 1, pp. 27 - 32
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2014, Volume 370, Issue 9, pp. 799 - 808
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
15.