| 000 | 01615 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250517232123.0 | ||
| 264 | 0 | _c20190625 | |
| 008 | 201906s 0 0 eng d | ||
| 022 | _a1559-0755 | ||
| 024 | 7 |
_a10.1007/s12026-018-9019-2 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMarcus, Nufar | |
| 245 | 0 | 0 |
_aMHC II deficient infant identified by newborn screening program for SCID. _h[electronic resource] |
| 260 |
_bImmunologic research _c08 2018 |
||
| 300 |
_a537-542 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aCD4-Positive T-Lymphocytes _xphysiology |
| 650 | 0 | 4 | _aChimerism |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aHLA-DR Antigens _xgenetics |
| 650 | 0 | 4 | _aHematopoietic Stem Cell Transplantation |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aIsrael |
| 650 | 0 | 4 | _aLymphopenia |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aNeonatal Screening |
| 650 | 0 | 4 |
_aReceptors, Antigen, T-Cell _xgenetics |
| 650 | 0 | 4 |
_aRegulatory Factor X Transcription Factors _xgenetics |
| 650 | 0 | 4 |
_aSevere Combined Immunodeficiency _xdiagnosis |
| 650 | 0 | 4 | _aExome Sequencing |
| 700 | 1 | _aStauber, Tali | |
| 700 | 1 | _aLev, Atar | |
| 700 | 1 | _aSimon, Amos J | |
| 700 | 1 | _aStein, Jerry | |
| 700 | 1 | _aBroides, Arnon | |
| 700 | 1 | _aSomekh, Ido | |
| 700 | 1 | _aAlmashanu, Shlomo | |
| 700 | 1 | _aSomech, Raz | |
| 773 | 0 |
_tImmunologic research _gvol. 66 _gno. 4 _gp. 537-542 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s12026-018-9019-2 _zAvailable from publisher's website |
| 999 |
_c28706816 _d28706816 |
||