000 01059 a2200337 4500
005 20250511124503.0
264 0 _c19791024
008 197910s 0 0 eng d
022 _a0340-6717
024 7 _a10.1007/BF00295596
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFleischman, E W
245 0 0 _aChromosomal marker 20q- in cases of osteomyelosclerosis and CML.
_h[electronic resource]
260 _bHuman genetics
_c1979
300 _a101-4 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAged
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, 19-20
650 0 4 _aErythropoiesis
650 0 4 _aHumans
650 0 4 _aLeukemia, Myeloid
_xgenetics
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPrimary Myelofibrosis
_xgenetics
700 1 _aPrigogina, E L
700 1 _aVolkova, M A
700 1 _aKulagina, O E
773 0 _tHuman genetics
_gvol. 50
_gno. 1
_gp. 101-4
856 4 0 _uhttps://doi.org/10.1007/BF00295596
_zAvailable from publisher's website
999 _c313979
_d313979