000 01744 a2200445 4500
005 20250511195222.0
264 0 _c19920910
008 199209s 0 0 eng d
022 _a0007-1048
024 7 _a10.1111/j.1365-2141.1992.tb08223.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aParlier, V
245 0 0 _aTrisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria.
_h[electronic resource]
260 _bBritish journal of haematology
_cJun 1992
300 _a296-304 p.
_bdigital
500 _aPublication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAnemia, Sideroblastic
_xetiology
650 0 4 _aChromosomes, Human, Pair 8
650 0 4 _aDNA
_xanalysis
650 0 4 _aErythrocytes
_xultrastructure
650 0 4 _aGranulocytes
_xultrastructure
650 0 4 _aHemoglobinuria, Paroxysmal
_xcomplications
650 0 4 _aHistocytological Preparation Techniques
650 0 4 _aHumans
650 0 4 _aImmunohistochemistry
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aMegakaryocytes
_xultrastructure
650 0 4 _aMonocytes
_xultrastructure
650 0 4 _aNucleic Acid Hybridization
650 0 4 _aTrisomy
700 1 _aTiainen, M
700 1 _aBeris, P
700 1 _aMiescher, P A
700 1 _aKnuutila, S
700 1 _aJotterand Bellomo, M
773 0 _tBritish journal of haematology
_gvol. 81
_gno. 2
_gp. 296-304
856 4 0 _uhttps://doi.org/10.1111/j.1365-2141.1992.tb08223.x
_zAvailable from publisher's website
999 _c1649506
_d1649506