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02932nam a22002895i 4500 |
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20201012140104.0 |
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cr nn 008mamaa |
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181130s2019 xxu| s |||| 0|eng d |
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|a 9781493988891
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| 024 |
7 |
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|a 10.1007/978-1-4939-8889-1
|2 doi
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| 040 |
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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| 245 |
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|a Prenatal Diagnosis /
|c edited by Brynn Levy.
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| 250 |
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|a 2nd ed. 2019.
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| 260 |
# |
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|a New York, NY :
|b Springer New York :
|b Imprint: Humana,
|c 2019.
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| 300 |
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|a XI, 363 p. 35 illus., 28 illus. in color. :
|b online resource.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a Methods in Molecular Biology,
|v 1885
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| 505 |
0 |
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|a Traditional Prenatal Diagnosis: Past to Present -- Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction -- Non-Invasive Approaches to Prenatal Diagnosis: Historical Perspective and Future Directions -- Molecular Testing for Preimplantation Genetic Diagnosis of Single Gene Disorders -- Detection of Aneuploidy and Unbalanced Rearrangements using Comparative Genomic Hybridization Microarrays -- Aneuploidy Screening using Next Generation Sequencing -- DNA Extraction from Various Types of Prenatal Specimens -- Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR) -- Rapid Prenatal Aneuploidy Screening by Fluorescence In Situ Hybridization (FISH) -- Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence PCR -- Multiplex Ligation-Dependent Probe Amplification (MLPA) for Prenatal Diagnosis of Common Aneuploidies -- Chromosomal Microarray Analysis using Array Comparative Genomic Hybridization on DNA from Amniotic Fluid and Chorionic Villus Sampling -- Prenatal Diagnosis using Chromosomal SNP Microarrays -- Rapid Detection of Fetal Mendelian Disorders: Thalassemia and Sickle Cell Syndromes -- Prenatal Diagnosis of Cystic Fibrosis -- Prenatal Diagnosis of Tay-Sachs Disease -- Next-Generation Sequencing of Prenatal Structural Chormosomal Rearrangements using Large-Insert Libraries -- Prenatal Diagnosis by Whole Exome Sequencing in Fetuses with Ultrasound Abnormalities -- 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 PRA -- Isolation of Cell-Free DNA from Maternal Plasma -- Noninvasive Detection of Fetal Aneuploidy using Next-Generation Sequencing -- Noninvasive Antenatal Screening for Fetal RHD in RhD Negative Women to Guide Targeted Anti-D Prophylaxis.
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| 650 |
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|a Molecular biology.
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| 650 |
1 |
4 |
|a Molecular Medicine.
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| 700 |
1 |
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|a Levy, Brynn.
|e editor.
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| 710 |
2 |
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|a SpringerLink (Online service)
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| 773 |
0 |
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|t Springer eBooks
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| 900 |
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|a Libro descargado a ALEPH en bloque (proveniente de proveedor)
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