000			01628 a2200493 4500
005			20250513041402.0
264		0	_c19950525
008			199505s 0 0 eng d
022			_a0006-4971
040			_aNLM _beng _cNLM
100	1		_aLuna-Fineman, S
245	0	0	_aChildhood monosomy 7: epidemiology, biology, and mechanistic implications. _h[electronic resource]
260			_bBlood _cApr 1995
300			_a1985-99 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.; Review
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aChromosome Aberrations _xepidemiology
650	0	4	_aChromosome Deletion
650	0	4	_aChromosome Disorders
650	0	4	_aChromosomes, Human, Pair 7
650	0	4	_aFemale
650	0	4	_aGenes, Neurofibromatosis 1
650	0	4	_aGenes, ras
650	0	4	_aGenetic Diseases, Inborn _xgenetics
650	0	4	_aGenetic Predisposition to Disease
650	0	4	_aHematopoietic Stem Cells _xpathology
650	0	4	_aHumans
650	0	4	_aIncidence
650	0	4	_aInfant
650	0	4	_aInfant, Newborn
650	0	4	_aLeukemia, Myeloid _xclassification
650	0	4	_aLeukemia, Radiation-Induced _xgenetics
650	0	4	_aMale
650	0	4	_aMonosomy
650	0	4	_aMyelodysplastic Syndromes _xclassification
650	0	4	_aNeoplasms, Second Primary _xchemically induced
650	0	4	_aRisk
700	1		_aShannon, K M
700	1		_aLange, B J
773	0		_tBlood _gvol. 85 _gno. 8 _gp. 1985-99
999			_c7718260 _d7718260