JIMD Reports . Volume 13 Case and Research Reports / edited by Johannes Zschocke, K. Michael Gibson, Garry Brown, Eva Morava, Verena Peters.
Contributor(s): SpringerLink (Online service)
| Zschocke, Johannes, editor literario | Gibson, K. Michael, editor literario | Brown, Garry, editor literario | Morava, Eva, editor literario | Peters, Verena, editor literario
Material type: 
E-bookSeries: JIMD Reports; 1313Publisher: Berlin, Heidelberg : Springer, 2014Description: 1 recurso en línea (VI, 167 p.) : 55 ilustraciones, 30 ilustraciones en color.ISBN: 9783642541490.Subject: Metabolismo -- Trastornos | Metabolismo -- Trastornos | Medicina | Fisiología humana | Fisiología humana | Genética humana | Genética humana | Pediatría | PediatríaDDC classification: 611.01816 | 599.935 Online resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)
Summary: 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.
| Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds | |
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Madrid Digital Acceso Electrónico (UEM) | Ciencias de la Salud | RC627.8 J563 2014 EB (Browse shelf(Opens below)) | .i11563084 | Acceso electrónico | eBOOK .i11563084 |
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| RC627.8 .J55 2015 EB JIMD Reports Volume 29 | RC627.8 .J55 2015 EB JIMD Reports Volume 24 | RC627.8 J563 2014 EB JIMD Reports Volume 12 | RC627.8 J563 2014 EB JIMD Reports Volume 13 Case and Research Reports | RC627.8 J563 2014 EB JIMD Reports Volume 14 | RC627.8 J563 2015 EB JIMD Reports Volume 15 | RC627.8 .J563 2015 EB JIMD Reports Volume 20 |
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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