| 000 | 01559 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250513022502.0 | ||
| 264 | 0 | _c19800726 | |
| 008 | 198007s 0 0 eng d | ||
| 022 | _a0009-9163 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.1980.tb00150.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAitken, D A | |
| 245 | 0 | 0 |
_aPrenatal detection of a probable heterozygote for ADA deficiency and severe combined immunodeficiency disease using a microradioassay. _h[electronic resource] |
| 260 |
_bClinical genetics _cApr 1980 |
||
| 300 |
_a293-8 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAdenosine Deaminase _xblood |
| 650 | 0 | 4 |
_aAmniotic Fluid _xcytology |
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 |
_aErythrocytes _xenzymology |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFetal Blood _xenzymology |
| 650 | 0 | 4 |
_aFibroblasts _xenzymology |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aImmunologic Deficiency Syndromes _xenzymology |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMicrochemistry |
| 650 | 0 | 4 |
_aNucleoside Deaminases _xdeficiency |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 | _aPrenatal Diagnosis |
| 650 | 0 | 4 |
_aProtein Deficiency _xdiagnosis |
| 700 | 1 | _aKleijer, W J | |
| 700 | 1 | _aNiermeijer, M F | |
| 700 | 1 | _aHerbschleb-Voogt, E | |
| 700 | 1 | _aGaljaard, H | |
| 773 | 0 |
_tClinical genetics _gvol. 17 _gno. 4 _gp. 293-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.1980.tb00150.x _zAvailable from publisher's website |
| 999 |
_c7370732 _d7370732 |
||