| 000 | 01528 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250514032155.0 | ||
| 264 | 0 | _c20020523 | |
| 008 | 200205s 0 0 eng d | ||
| 022 | _a1077-4114 | ||
| 024 | 7 |
_a10.1097/00043426-200203000-00013 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSlayton, William B | |
| 245 | 0 | 0 |
_aLineage-specific trisomy 21 in a neonate with resolving transient myeloproliferative syndrome. _h[electronic resource] |
| 260 |
_bJournal of pediatric hematology/oncology _c |
||
| 300 |
_a224-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aAntigens, CD _xmetabolism |
| 650 | 0 | 4 |
_aCell Lineage _xgenetics |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 21 _xgenetics |
| 650 | 0 | 4 |
_aDown Syndrome _xgenetics |
| 650 | 0 | 4 | _aErythrocytes |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHematopoietic Stem Cells |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMonocytes |
| 650 | 0 | 4 |
_aMosaicism _xgenetics |
| 650 | 0 | 4 |
_aMyeloproliferative Disorders _xgenetics |
| 700 | 1 | _aSpangrude, Gerald J | |
| 700 | 1 | _aChen, Zhong | |
| 700 | 1 | _aGreene, Wayne F | |
| 700 | 1 | _aVirshup, David | |
| 773 | 0 |
_tJournal of pediatric hematology/oncology _gvol. 24 _gno. 3 _gp. 224-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1097/00043426-200203000-00013 _zAvailable from publisher's website |
| 999 |
_c11889890 _d11889890 |
||