| 000 | 01057nam a2200313 a 4500 | ||
|---|---|---|---|
| 005 | 20250918170804.0 | ||
| 008 | 121008s2011 xxka 001 0 eng | ||
| 020 |
_a9780195379631 _cRM168.25 |
||
| 039 | 9 |
_a201302210846 _bzaleha _c201302131658 _dIzzati _y10-08-2012 _zbalqis |
|
| 040 | _dUKM | ||
| 090 | _aQU500.S655p 2011 9HUKM | ||
| 090 |
_aQU500 _b.S655p 2011 9HUKM |
||
| 100 | 1 | _aSmith, Moyra. | |
| 245 | 1 | 0 |
_aPhenotypic variation : _bexploration and functional genomics / _cMoyra Smith. |
| 260 |
_aOxford : _bOxford University Press, _c2011. |
||
| 300 |
_axii, 240 p. : _bill. ; _c24 cm. |
||
| 650 | 2 | _aGenetic Variation. | |
| 650 | 2 | _aPhenotype. | |
| 650 | 2 | _aGenomics. | |
| 650 | 2 |
_aCongenital Abnormalities _xgenetics. |
|
| 650 | 2 |
_aNervous System Diseases _xgenetics. |
|
| 907 |
_a.b15496880 _b2019-11-12 _c2019-11-12 |
||
| 942 |
_c01 _n0 _kQU500.S655p 2011 9HUKM |
||
| 914 | _avtls003515200 | ||
| 990 | _aNHR/za | ||
| 991 | _aJabatan Makmal Diagnostik, PPUKM | ||
| 998 |
_ah _b2012-08-10 _cm _da _feng _gxxk _y0 _z.b15496880 |
||
| 999 |
_c532822 _d532822 |
||