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120106s2012 xxu| s |||| 0|eng d |
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|a 9781617795077
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|a 10.1007/978-1-61779-507-7
|2 doi
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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|a Genomic Structural Variants :
|b Methods and Protocols /
|c edited by Lars Feuk.
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250 |
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|a 1st ed. 2012.
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|a Totowa, NJ :
|b Humana Press :
|b Imprint: Humana,
|c 2012.
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|a XI, 386 p. 39 illus., 5 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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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a Methods in Molecular Biology,
|v 838
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|a What Have Studies of Genomic Disorders Taught us about our Genome -- Microdeletion and Microduplication Syndromes -- Structural Genomic Variation in Mental Retardation -- Copy Number Variation and Psychiatric Disease Risk -- Detection and Characterization of Copy Number Variation (CNV) in Autism Spectrum Disorder (ASD) -- Structural Variation in Subtelomeres -- Array Based Approaches in Prenatal Diagnosis -- Structural Variation and its Effect on Expression -- The Challenges of Studying Complex and Dynamic Regions of the Human Genome -- Population Genetic Nature of Copy Number Variation -- Detection and Interpretation of Genomic Structural Variation in Mammals -- Structural Genetic Variation in the Context of Somatic Mosaicism -- Online Resources for Genomic Structural Variation -- Algorithm Implementation for CNV Discovery using Affymetrix and Ilumina SNP Array Data -- Targeted Screening and Validation of Copy Nuber Variations -- High-resolution Copy Number Profiling by Array CGH using DNA Isolated from Formalin-Fixed Paraffin-Embedded Tissues -- Characterizing and Interpreting Genetic Variation from Personal Genome Sequencing -- Massively Parallel Sequencing Approaches for Characterization of Structural Variation.
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|a Human genetics.
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|a Medical genetics.
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|a Human Genetics.
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|a Gene Function.
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|a Feuk, Lars.
|e editor.
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710 |
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|a SpringerLink (Online service)
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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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