Founder mutations in inherited cardiac diseases in the Netherlands / edited by Arthur A.M. Wilde, J. Peter Tintelen.
Contributor(s): SpringerLink (Online service)
| Wilde, Arthur A.M, editor literario | Tintelen, J. Peter, editor literario
Material type: 
E-bookPublisher: Houten : Bohn Stafleu van Loghum Imprint: Bohn Stafleu van Loghum, 2014Description: 1 recurso en línea (IX, 102 p.) :.ISBN: 9789036807050.Subject: Cardiología | Medicina | Genética humana | Genética humanaDDC classification: 611.01816 | 599.935 Online resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)
Summary: This booklet summarizes our current knowledge of founder mutation populations (â€ẽxtended familiesâ€{u9829}n the Netherlands, among other aspects providing insight in where these patients can be expected (coloured maps of the prevalence in the 99 Dutch postal code regions are provided for every phenotype) and what their precise phenotype is.
| Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds | |
|---|---|---|---|---|---|---|---|---|---|
LIBRO-E NO PRÉSTAMO
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Madrid Digital Acceso Electrónico (UEM) | Ciencias de la Salud | RB155-155.8 EB (Browse shelf(Opens below)) | .i11564404 | Acceso electrónico | eBOOK .i11564404 |
Total holds: 0
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| RB1-214 Pathology of the Ovary, Fallopian Tube and Peritoneum | RB1-214 EB Diagnostic Cytopathology Board Review and Self-Assessment | RB155-155.8 Clinical Metabolomics Applications in Genetic Diseases | RB155-155.8 EB Founder mutations in inherited cardiac diseases in the Netherlands | RB155-155.8 EB JIMD Reports Volume 18 | RB155-155.8 EB JIMD Reports Volume 19 | RB155-155.8 EB JIMD Reports Volume 22 |
This booklet summarizes our current knowledge of founder mutation populations (â€ẽxtended familiesâ€{u9829}n the Netherlands, among other aspects providing insight in where these patients can be expected (coloured maps of the prevalence in the 99 Dutch postal code regions are provided for every phenotype) and what their precise phenotype is.
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