| 000 | 01573 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250517234624.0 | ||
| 264 | 0 | _c20190107 | |
| 008 | 201901s 0 0 eng d | ||
| 022 | _a1472-4146 | ||
| 024 | 7 |
_a10.1136/jclinpath-2018-205235 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aArun, A Kumar | |
| 245 | 0 | 0 |
_aSpectrum of _h[electronic resource] |
| 260 |
_bJournal of clinical pathology _cDec 2018 |
||
| 300 |
_a1046-1050 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 | _aDatabases, Genetic |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFrameshift Mutation |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIndia |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aLeukocyte Elastase _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aNeutropenia _xcongenital |
| 650 | 0 | 4 |
_aNeutrophils _xpathology |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aSenthamizhselvi, Anandan | |
| 700 | 1 | _aHemamalini, Suresh | |
| 700 | 1 | _aEdison, Eunice S | |
| 700 | 1 | _aKorula, Anu | |
| 700 | 1 | _aFouzia, N A | |
| 700 | 1 | _aGeorge, Biju | |
| 700 | 1 | _aMathews, Vikram | |
| 700 | 1 | _aBalasubramanian, Poonkuzhali | |
| 773 | 0 |
_tJournal of clinical pathology _gvol. 71 _gno. 12 _gp. 1046-1050 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jclinpath-2018-205235 _zAvailable from publisher's website |
| 999 |
_c28792098 _d28792098 |
||