JIMD Reports . Volume 24 / edited by Johannes Zschocke, Matthias Baumgartner, Eva Morava, Marc Patterson, Shamima Rahman, Verena Peters.
Contributor(s): Baumgartner, Matthias R., editor literario
| Morava, Eva, editor literario | Patterson, Marc, editor literario | Peters, Verena, editor literario | Rahman, Shamima, editor literario | Zschocke, Johannes, editor literario | SpringerLink (Online service)
Material type: 
E-bookSeries: (JIMD Reports, 2192-8304; 24).Publisher: Berlin, Heidelberg : Springer, 2015Description: 1 recurso en línea (VI, 128 páginas) : 30 ilustraciones, 10 ilustraciones en color.ISBN: 9783662482278.Subject: Enfermedades hereditarias metabólicasDDC classification: 612 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 | |
|---|---|---|---|---|---|---|---|---|---|
LIBRO-E NO PRÉSTAMO
|
Madrid Digital Acceso Electrónico (UEM) | Ciencias de la Salud | RC627.8 .J55 2015 EB (Browse shelf(Opens below)) | .i11571299 | Acceso electrónico | eBOOK .i11571299 |
Total holds: 0
Browsing Madrid Digital shelves, Shelving location: Acceso Electrónico (UEM) Close shelf browser (Hides shelf browser)
| RC627.8 I536 2016 EB Inborn Metabolic Diseases : Diagnosis and Treatment | RC627.8 I544 2017 EB Inherited metabolic diseases : a clinical approach | 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 |
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.
There are no comments on this title.
Log in to your account to post a comment.