| 000 | 01341 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250512023804.0 | ||
| 264 | 0 | _c19880401 | |
| 008 | 198804s 0 0 eng d | ||
| 022 | _a0140-6736 | ||
| 024 | 7 |
_a10.1016/s0140-6736(88)91234-2 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKattamis, C | |
| 245 | 0 | 0 |
_aCorrelation of clinical phenotype to genotype in haemoglobin H disease. _h[electronic resource] |
| 260 |
_bLancet (London, England) _cFeb 1988 |
||
| 300 |
_a442-4 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 |
_aDNA Restriction Enzymes _xanalysis |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aHemoglobin H _xanalysis |
| 650 | 0 | 4 |
_aHemoglobins, Abnormal _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aThalassemia _xgenetics |
| 700 | 1 | _aTzotzos, S | |
| 700 | 1 | _aKanavakis, E | |
| 700 | 1 | _aSynodinos, J | |
| 700 | 1 | _aMetaxotou-Mavrommati, A | |
| 773 | 0 |
_tLancet (London, England) _gvol. 1 _gno. 8583 _gp. 442-4 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0140-6736(88)91234-2 _zAvailable from publisher's website |
| 999 |
_c2899715 _d2899715 |
||