000			01953 a2200625 4500
005			20250513230354.0
264		0	_c20010607
008			200106s 0 0 eng d
022			_a0964-6906
024	7		_a10.1093/hmg/10.4.339 _2doi
040			_aNLM _beng _cNLM
100	1		_aDaniels, R J
245	0	0	_aSequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16. _h[electronic resource]
260			_bHuman molecular genetics _cFeb 2001
300			_a339-52 p. _bdigital
500			_aPublication Type: Case Reports; Comparative Study; Journal Article
650	0	4	_aAdolescent
650	0	4	_aAnimals
650	0	4	_aAsthma _xgenetics
650	0	4	_aBase Composition
650	0	4	_aBipolar Disorder _xgenetics
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aChromosomes, Human, Pair 16 _xchemistry
650	0	4	_aCpG Islands _xgenetics
650	0	4	_aEpilepsy _xgenetics
650	0	4	_aFemale
650	0	4	_aGenetic Linkage _xgenetics
650	0	4	_aHumans
650	0	4	_aIntellectual Disability _xgenetics
650	0	4	_aMale
650	0	4	_aMice
650	0	4	_aMonosomy
650	0	4	_aPhenotype
650	0	4	_aPhysical Chromosome Mapping
650	0	4	_aPolycystic Kidney, Autosomal Dominant _xgenetics
650	0	4	_aRecombination, Genetic
650	0	4	_aSequence Analysis, DNA
650	0	4	_aSyndrome
650	0	4	_aTelomere _xchemistry
650	0	4	_aTuberous Sclerosis _xgenetics
650	0	4	_aalpha-Thalassemia _xgenetics
700	1		_aPeden, J F
700	1		_aLloyd, C
700	1		_aHorsley, S W
700	1		_aClark, K
700	1		_aTufarelli, C
700	1		_aKearney, L
700	1		_aBuckle, V J
700	1		_aDoggett, N A
700	1		_aFlint, J
700	1		_aHiggs, D R
773	0		_tHuman molecular genetics _gvol. 10 _gno. 4 _gp. 339-52
856	4	0	_uhttps://doi.org/10.1093/hmg/10.4.339 _zAvailable from publisher's website
999			_c11097388 _d11097388