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Prenatal diagnosis / 2nd ed

Prenatal diagnosis / 2nd ed

Levy, Brynn.
서명 / 저자사항
Prenatal diagnosis / edited by Brynn Levy.
2nd ed.
New York :   Humana Press :   Springer,   c2019.  
xi, 363 p. : ill. (some col.) ; 27 cm.
Methods in molecular biology,1064-3745 ; 1885
Includes bibliographical references and index.
Prenatal diagnosis. Fetus --Diseases --Molecular diagnosis. Prenatal Diagnosis --methods. Fetal Diseases --diagnosis. Prenatal Diagnosis --trends.
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001 000046025687
005 20200424104919
008 200423s2019 nyua b 001 0 eng d
020 ▼a 9781493988877
040 ▼a 211009 ▼c 211009 ▼d 211009
082 0 4 ▼a 618.32075 ▼2 23
084 ▼a 618.32075 ▼2 DDCK
090 ▼a 618.32075 ▼b P926-2
245 0 0 ▼a Prenatal diagnosis / ▼c edited by Brynn Levy.
250 ▼a 2nd ed.
260 ▼a New York : ▼b Humana Press : ▼b Springer, ▼c c2019.
300 ▼a xi, 363 p. : ▼b ill. (some col.) ; ▼c 27 cm.
490 1 ▼a Methods in molecular biology, ▼x 1064-3745 ; ▼v 1885
490 1 ▼a Springer protocols
504 ▼a Includes bibliographical references and index.
650 0 ▼a Prenatal diagnosis.
650 0 ▼a Fetus ▼x Diseases ▼x Molecular diagnosis.
650 1 2 ▼a Prenatal Diagnosis ▼x methods.
650 2 2 ▼a Fetal Diseases ▼x diagnosis.
650 2 2 ▼a Prenatal Diagnosis ▼x trends.
700 1 ▼a Levy, Brynn.
830 0 ▼a Methods in molecular biology ; ▼v 1885.
830 0 ▼a Springer protocols.
945 ▼a KLPA


No. 소장처 청구기호 등록번호 도서상태 반납예정일 예약 서비스
No. 1 소장처 과학도서관/Sci-Info(2층서고)/ 청구기호 618.32075 P926-2 등록번호 121253040 도서상태 대출가능 반납예정일 예약 서비스 B M



Preface...Table of Contents...Contributing Authors....
Part I Historical Introduction
1. Traditional Prenatal Diagnosis: Past to PresentBrynn Levy and Melissa Stosic
2. Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future DirectionJoe Leigh Simpson, Anver Kuliev, and Svetlana Rechitsky
3. Non-Invasive Approaches to Prenatal Diagnosis: Historical Perspective and Future DirectionsLisa Hui
Part II Preimplantation Genetic Testing
4. Molecular Testing for Preimplantation Genetic Diagnosis of Single Gene DisordersRebekah S. Zimmerman, Jennifer Eccles, Chaim Jalas, Nathan R. Treff, and Richard T. Scott, Jr.
5. Detection of Aneuploidy and Unbalanced Rearrangements using Comparative Genomic Hybridization MicroarraysLorena Rodrigo and Carmen Rubio
6. Aneuploidy Screening using Next Generation SequencingCengiz Cinnioglu, Refik Kayali, Tristan Darvin, Adedoyin Akinwole, Milena Jaukowska, and Gary Harton
Part III Traditional Prenatal Diagnosis
7. DNA Extraction from Various Types of Prenatal SpecimensOdelia Nahum, Amanda Thomas, and Brynn Levy
8. Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR)Christie Buchovecky, Odelia Nahum, and Brynn Levy
9. Rapid Prenatal Aneuploidy Screening by Fluorescence In Situ Hybridization (FISH)Anja Weise and Thomas Liehr
10. Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence PCRKathy Mann, Erwin Petek, and Barbara Pertl
11. Multiplex Ligation-Dependent Probe Amplification (MLPA) for Prenatal Diagnosis of Common AneuploidiesJan Schouten, Paul van Vught, and Robert-Jan Galjaard
12. Chromosomal Microarray Analysis using Array Comparative Genomic Hybridization on DNA from Amniotic Fluid and Chorionic Villus SamplingAnkita Patel
13. Prenatal Diagnosis using Chromosomal SNP MicroarraysMythily Ganapathi, Odelia Nahum, and Brynn Levy
14. Rapid Detection of Fetal Mendelian Disorders: Thalassemia and Sickle Cell SyndromesJoanne Traeger-Synodinos, Christina Vrettou, and Emmanuel Kanavakis
15. Prenatal Diagnosis of Cystic FibrosisAnastasia M. Fedick, Jinglan Zhang, Lisa Edelmann, and Ruth Kornreich
16. Prenatal Diagnosis of Tay-Sachs DiseaseJinglan Zhang, Hongjie Chen, Ruth Kornreich, and Chunli Yu
17. Next-Generation Sequencing of Prenatal Structural Chormosomal Rearrangements using Large-Insert LibrariesBenjamin B. Currall, Caroline W. Antolik, Ryan L. Collins, and Michael E. Talkowski
18. Prenatal Diagnosis by Whole Exome Sequencing in Fetuses with Ultrasound AbnormalitiesVanessa Felice, Avinash Abhayankar, and Vaidehi Jobanputra
Part IV Non-Invasive Prenatal Testing
19. Quad Screen Test, A Multiplexed Biomarker Assay for Prenatal Screening to Assess Birth Defects: The Columbia University Experience using the Beckman Access2 Immunoassay Analyzer and Benetech PRAAwet Tecleab, Alex Lyashchenko, and Alex J. Rai
20. Isolation of Cell-Free DNA from Maternal PlasmaJames Stray and Bernhard Zimmermann
21. Noninvasive Detection of Fetal Aneuploidy using Next-Generation SequencingKirsten J. Curnow, Rebecca K. Sanderson, and Sue Beruti
22. Noninvasive Antenatal Screening for Fetal RHD in RhD Negative Women to Guide Targeted Anti-D ProphylaxisFrederik Banch Clausen, Klaus Rieneck, Grethe Risum Krog, Birgitte Suhr Bundgaard, and Morten Hanefeld Dziegiel

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