JIMD Reports - Case and Research Reports, 2011/1 [recurso electrónico] : Case and Research Reports.
Tipo de material:
TextoSeries JIMD Reports ; 1Editor: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2011Edición: FirstDescripción: VI, 136 p. 27 illus., 9 illus. in color. online resourceTipo de contenido: text Tipo de medio: computer Tipo de portador: online resourceISBN: 9783642177088Tema(s): Medicine | Human genetics | Human physiology | Metabolic diseases | Pediatrics | Biomedicine | Human Genetics | Metabolic Diseases | Pediatrics | Human PhysiologyFormatos físicos adicionales: Printed edition:: Sin títuloClasificación CDD: 611.01816 | 599.935 Clasificación LoC:RB155-155.8QH431Recursos en línea: Libro electrónico
En: Springer eBooksResumen: 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.
| Tipo de ítem | Biblioteca actual | Colección | Signatura | Copia número | Estado | Fecha de vencimiento | Código de barras |
|---|---|---|---|---|---|---|---|
| Libro Electrónico | Biblioteca Electrónica | Colección de Libros Electrónicos | RB155 -155.8 (Browse shelf(Abre debajo)) | 1 | No para préstamo | 375574-2001 |
Navegando Biblioteca Electrónica Estantes, Código de colección: Colección de Libros Electrónicos Cerrar el navegador de estanterías (Oculta el navegador de estanterías)
| RB155 -155.8 Molecular Basis of Multiple Sclerosis | RB155 -155.8 Epigenetics and Human Reproduction | RB155 -155.8 Brain, Behavior and Epigenetics | RB155 -155.8 JIMD Reports - Case and Research Reports, 2011/1 | RB155 -155.8 Is this Cell a Human Being? | RB155 -155.8 Epigenetics and Disease | RB155 -155.8 Genome Stability and Human Diseases |
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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