| 000 | 00949 a2200301 4500 | ||
|---|---|---|---|
| 005 | 20250514153344.0 | ||
| 264 | 0 | _c19981101 | |
| 008 | 199811s 0 0 eng d | ||
| 022 | _a0006-4971 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSCOTT, J L | |
| 245 | 0 | 0 |
_aCongenital hemolytic disease associated with red cell inclusion bodies, abnormal pigment metabolism and an electrophoretic hemoglobin abnormality. _h[electronic resource] |
| 260 |
_bBlood _cSep 1960 |
||
| 300 |
_a1239-52 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAnemia |
| 650 | 0 | 4 | _aAnemia, Hemolytic |
| 650 | 0 | 4 | _aErythrocytes |
| 650 | 0 | 4 | _aHemoglobins |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInclusion Bodies |
| 650 | 0 | 4 | _aMedical Records |
| 650 | 0 | 4 |
_aPigments, Biological _xmetabolism |
| 700 | 1 | _aHAUT, A | |
| 700 | 1 | _aCARTWRIGHT, G E | |
| 700 | 1 | _aWINTROBE, M M | |
| 773 | 0 |
_tBlood _gvol. 16 _gp. 1239-52 |
|
| 999 |
_c14205971 _d14205971 |
||