|
|
|
|
LEADER |
01816nam a22002775i 4500 |
001 |
000279095 |
005 |
20211026202830.0 |
007 |
cr nn 008mamaa |
008 |
100301s2007 xxu| s |||| 0|eng d |
020 |
|
|
|a 9781597451598
|
024 |
7 |
|
|a 10.1007/978-1-59745-159-8
|2 doi
|
040 |
|
|
|a Sistema de Bibliotecas del Tecnológico de Costa Rica
|
245 |
1 |
0 |
|a Cardiovascular Disease, Volume 1 :
|b Genetics /
|c edited by Qing Wang.
|
250 |
|
|
|a 1st ed. 2007.
|
260 |
# |
# |
|a Totowa, NJ :
|b Humana Press :
|b Imprint: Humana,
|c 2007.
|
300 |
|
|
|a XII, 238 p. 154 illus., 11 illus. in color. :
|b online resource.
|
336 |
|
|
|a text
|b txt
|2 rdacontent
|
337 |
|
|
|a computer
|b c
|2 rdamedia
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
490 |
1 |
|
|a Methods in Molecular Medicine,
|v 128
|
505 |
0 |
|
|a Cytogenetic Analysis of Cardiovascular Disease -- Fluorescence In Situ Hybridization in Cardiovascular Disease -- Comparative Genomic Hybridization by Microarray for the Detection of Cytogenetic Imbalance -- Construction of Somatic Cell Hybrid Lines -- LINKAGE Programs -- SAGE Programs -- Linkage Analysis for Complex Diseases Using Variance Component Analysis -- Genome Resources and Comparative Analysis Tools for Cardiovascular Research -- Positional Cloning -- Positional Cloning -- Chromosome Substitution Strains -- Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms Conferring Risk of Myocardial Infarction -- Mutation Detection in Congenital Long QT Syndrome -- High-Throughput Single-Nucleotide Polymorphisms Genotyping -- Genotyping Single-Nucleotide Polymorphisms by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight-Based Mini-Sequencing.
|
650 |
|
0 |
|a Cardiology.
|
650 |
1 |
4 |
|a Cardiology.
|
700 |
1 |
|
|a Wang, Qing.
|e editor.
|
710 |
2 |
|
|a SpringerLink (Online service)
|
773 |
0 |
|
|t Springer eBooks
|