| 000 | 02782cam a2200421Ii 4500 | ||
|---|---|---|---|
| 001 | 96317 | ||
| 003 | ES-MaUEC | ||
| 005 | 20230102112748.0 | ||
| 006 | m o d | ||
| 007 | cr cnu|||unuuu | ||
| 008 | 170711s2017 sz a ob 000 0 eng d | ||
| 020 | _a331954098X | ||
| 020 |
_a3319540998 _q(electronic bk.) |
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| 020 | _a9783319540986 | ||
| 020 |
_a9783319540993 _q(electronic bk.) |
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| 020 |
_z9783319540986 _q(print) |
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| 040 |
_aN$T _cN$T _dEBLCP _dGW5XE _dN$T _dYDX _dOCLCF _dNJR _dUAB _dESU _dAZU _dUPM _dCOO _dOCLCQ _dMERER _dVT2 _dOCLCQ _dOCL _dIOG _dES-MaUEC _bspa |
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| 050 | 4 |
_aQH431 _b2017 EB |
|
| 245 | 0 | 0 |
_aHuman chromosome atlas : _bintroduction to diagnostics of structural aberrations _cClaudia Behrend, Javad Karimzad Hagh, Parvin Mehdipour, Gesa Schwanitz. |
| 264 | 1 |
_aCham, Switzerland _bSpringer _c[2017] |
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| 300 |
_a1 recurso en línea (viii, 207 páginas) _bilustraciones |
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| 336 |
_aTexto _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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| 338 |
_arecurso electrónico _bcr _2rdacarrier |
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| 347 |
_atext file _bPDF |
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| 500 |
_aSpringerLink _bSpringer Biomedical and Life Sciences eBooks 2017 English+International |
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| 504 | _aIncluye referencias bibliográficas | ||
| 505 | 0 | _aIntroduction -- Structural chromosome aberrations -- Mutations in non-coding-DNA regions -- Single case presentations -- Mutations in non-coding-DNA regions -- Outlook -- Bibliography. | |
| 520 | 3 | _aThis atlas presents the results of cases of structural chromosome aberrations based on the currently available methods of analysis for different types of abnormality. It particularly focuses on which spectrum should be chosen when combining the different techniques to achieve the best method of diagnosis in individual cases, for example direct preparation of cells and mitoses, short or long-time cell culture, fluorescence in situ hybridization (FISH), analysis of interphases, microarray or DNA sequencing. Generally it has to be taken into account, that the development of new and improved investigation methods is forthcoming. Thus, by improvement of diagnostic possibilities new fields of investigation arise, and special groups of patients with cytogenetic analyses can be re-analysed under new research questions. | |
| 650 | 7 |
_aCromosomas _2embne _0(OCoLC)fst00962918 _0 _9139992 |
|
| 700 | 1 |
_aBehrend, Claudia, _eautor |
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| 700 | 1 |
_aHagh, Javad Karimzad, _eautor |
|
| 700 | 1 |
_aMehdipour, Parvin, _eautor _994288 |
|
| 700 | 1 |
_aSchwanitz, Gesa, _eautor |
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| 856 | 4 | 0 |
_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=http://link.springer.com/10.1007/978-3-319-54099-3 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid) |
| 988 | _aEBOOK, asignarmaterias, EBSPRINGER_2017D | ||
| 998 |
_b02/2018 _dz _e- _zSI |
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| 999 |
_c96317 _d96317 _x1 |
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