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100301s2006 xxu| s |||| 0|eng d |
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|a 9781597450881
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| 024 |
7 |
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|a 10.1385/159745088X
|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 |
1 |
0 |
|a Congenital Heart Disease :
|b Molecular Diagnostics /
|c edited by Mary Kearns-Jonker.
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| 250 |
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|a 1st ed. 2006.
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| 260 |
# |
# |
|a Totowa, NJ :
|b Humana Press :
|b Imprint: Humana,
|c 2006.
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| 300 |
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|a X, 278 p. :
|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 Medicine,
|v 126
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| 505 |
0 |
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|a Genetics of Cardiac Septation Defects and Their Pre-Implantation Diagnosis -- Molecular and Genetic Aspects of DiGeorge/Velocardiofacial Syndrome -- Mutation Screening for the Genes Causing Cardiac Arrhythmias -- Mutation Analysis of the FBN1 Gene in Patients With Marfan Syndrome -- Mutation Analysis of PTPN11 in Noonan Syndrome by WAVE -- Williams-Beuren Syndrome Diagnosis Using Fluorescence In Situ Hybridization -- Congenital Heart Disease -- “Chip”ping Away at Heart Failure -- Molecular Diagnostics of Catecholaminergic Polymorphic Ventricular Tachycardia Using Denaturing High-Performance Liquid Chromatography and Sequencing -- Mutation Detection in Tumor Suppressor Genes Using Archival Tissue Specimens -- Friedreich Ataxia -- The Cardiovascular Manifestations of Alagille Syndrome and JAG1 Mutations -- Array Analysis Applied to Malformed Hearts -- DNA Mutation Analysis in Heterotaxy -- Use of Denaturing High-Performance Liquid Chromatography to Detect Mutations in Pediatric Cardiomyopathies.
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| 650 |
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0 |
|a Cardiology.
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| 650 |
1 |
4 |
|a Cardiology.
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| 700 |
1 |
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|a Kearns-Jonker, Mary.
|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)
|