000 | 01951nam a22005175i 4500 | ||
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001 | u375574 | ||
003 | SIRSI | ||
005 | 20160812084330.0 | ||
007 | cr nn 008mamaa | ||
008 | 110801s2011 gw | s |||| 0|eng d | ||
020 |
_a9783642177088 _9978-3-642-17708-8 |
||
040 | _cMX-MeUAM | ||
050 | 4 | _aRB155-155.8 | |
050 | 4 | _aQH431 | |
082 | 0 | 4 |
_a611.01816 _223 |
082 | 0 | 4 |
_a599.935 _223 |
110 | 2 |
_aSSIEM. _eeditor. |
|
245 | 1 | 0 |
_aJIMD Reports - Case and Research Reports, 2011/1 _h[recurso electrónico] : _bCase and Research Reports. |
250 | _aFirst. | ||
264 | 1 |
_aBerlin, Heidelberg : _bSpringer Berlin Heidelberg : _bImprint: Springer, _c2011. |
|
300 |
_aVI, 136 p. 27 illus., 9 illus. in color. _bonline resource. |
||
336 |
_atext _btxt _2rdacontent |
||
337 |
_acomputer _bc _2rdamedia |
||
338 |
_aonline resource _bcr _2rdacarrier |
||
347 |
_atext file _bPDF _2rda |
||
490 | 1 |
_aJIMD Reports, _x2192-8304 ; _v1 |
|
520 | _aJIMD 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. | ||
650 | 0 | _aMedicine. | |
650 | 0 | _aHuman genetics. | |
650 | 0 | _aHuman physiology. | |
650 | 0 | _aMetabolic diseases. | |
650 | 0 | _aPediatrics. | |
650 | 1 | 4 | _aBiomedicine. |
650 | 2 | 4 | _aHuman Genetics. |
650 | 2 | 4 | _aMetabolic Diseases. |
650 | 2 | 4 | _aPediatrics. |
650 | 2 | 4 | _aHuman Physiology. |
710 | 2 | _aSpringerLink (Online service) | |
773 | 0 | _tSpringer eBooks | |
776 | 0 | 8 |
_iPrinted edition: _z9783642177071 |
830 | 0 |
_aJIMD Reports, _x2192-8304 ; _v1 |
|
856 | 4 | 0 |
_zLibro electrónico _uhttp://148.231.10.114:2048/login?url=http://link.springer.com/book/10.1007/978-3-642-17708-8 |
596 | _a19 | ||
942 | _cLIBRO_ELEC | ||
999 |
_c203454 _d203454 |