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JIMD Reports . Volume 26 / edited by Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke, Verena Peters

Contributor(s): SpringerLink (Online service) | Morava, Eva, editor literario | Baumgartner, Matthias R., editor literario | Patterson, Marc, editor literario | Rahman, Shamima, editor literario | Zschocke, Johannes, editor literario | Peters, Verena, editor literario
Material type: materialTypeLabelE-bookSeries: JIMD Reports; 2626Publisher: Berlin, Heidelberg : Springer Berlin Heidelberg, 2016Edition: 1st ed.Description: 1 recurso en línea (VI, 113 p.) : 15 ilustraciones en color.ISBN: 9783662498330.Subject: Enfermedades hereditarias metabólicasDDC classification: 611.01816 | 599.935 Online resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources
Contents:
Chapter 1 -- Chapter 2 -- Chapter 3 -- Chapter 4 -- Chapter 5 -- Chapter 6 -- Chapter 7 -- Chapter 8 -- Chapter 9 -- Chapter 10 -- Chapter 11 -- Chapter 12 -- Chapter 13 -- Chapter 14 -- Chapter 15
Abstract: JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder
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Holdings
Item type Current library Collection Call number Copy number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC627.8 .J563 2016 EB (Browse shelf(Opens below)) .i11599777 Acceso electrónico eBOOK .i11599777
Total holds: 0

Chapter 1 -- Chapter 2 -- Chapter 3 -- Chapter 4 -- Chapter 5 -- Chapter 6 -- Chapter 7 -- Chapter 8 -- Chapter 9 -- Chapter 10 -- Chapter 11 -- Chapter 12 -- Chapter 13 -- Chapter 14 -- Chapter 15

JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder

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