| 000 | 01784 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250514204327.0 | ||
| 264 | 0 | _c20041015 | |
| 008 | 200410s 0 0 eng d | ||
| 022 | _a1474-547X | ||
| 024 | 7 |
_a10.1016/S0140-6736(04)17142-0 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDebiec, Hanna | |
| 245 | 0 | 0 |
_aRole of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies. _h[electronic resource] |
| 260 |
_bLancet (London, England) _c |
||
| 300 |
_a1252-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aAntigen-Antibody Complex _xanalysis |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFetal Diseases _xgenetics |
| 650 | 0 | 4 |
_aFetomaternal Transfusion _ximmunology |
| 650 | 0 | 4 |
_aGlomerulonephritis, Membranous _xcongenital |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aImmunization |
| 650 | 0 | 4 |
_aImmunoglobulin G _xanalysis |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIsoantibodies _ximmunology |
| 650 | 0 | 4 |
_aKidney Glomerulus _ximmunology |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNeprilysin _xdeficiency |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymerase Chain Reaction |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aPregnancy |
| 700 | 1 | _aNauta, Jeroen | |
| 700 | 1 | _aCoulet, Florence | |
| 700 | 1 | _avan der Burg, Mirjam | |
| 700 | 1 | _aGuigonis, Vincent | |
| 700 | 1 | _aSchurmans, Thierry | |
| 700 | 1 | _ade Heer, Emile | |
| 700 | 1 | _aSoubrier, Florent | |
| 700 | 1 | _aJanssen, Francoise | |
| 700 | 1 | _aRonco, Pierre | |
| 773 | 0 |
_tLancet (London, England) _gvol. 364 _gno. 9441 _gp. 1252-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/S0140-6736(04)17142-0 _zAvailable from publisher's website |
| 999 |
_c15155993 _d15155993 |
||