000			01667ngm a2200361 a 4500
001			HST2340_1_2
003			UkLoHST
006			m c
007			cr|cna|||a||||
007			vz|czazum
008			080121s2009 enk|||||||||||s|||v|eng d
028	5	0	_a2340 _bHenry Stewart Talks
035			_a(UkLoHST)1395
035			_a(UkLU-K)001155592
040			_aUkLU-K _beng _cUkLU-K
100	1		_aPonting, Chris, _u(University of Oxford, UK) _4spk
245	1	0	_aCNVs in human genomes _h[electronic resource] / _cChris Ponting.
260			_aLondon : _bHenry Stewart Talks, _c2009.
300			_a1 online resource (1 streaming video file (32 min.) : _bcolor, sound).
490	1		_aCopy number variation : expanding the repertoire of genetic alterations in studies of natural variation and disease, _x2056-452X
500			_aAnimated audio-visual presentation with synchonized narration.
500			_aTitle from title frames.
505	0		_aContents: Evolution of copy number variants -- Positive or negative selection acting on copy number variable genes -- Hill-Robertson interference and its effect on the efficacy of selection -- Prediction of genes more likely, when copy number variable, to contribute to human disease.
506			_aAccess restricted to subscribers.
538			_aMode of access: World Wide Web.
650		2	_aGene Dosage.
650		2	_aGenetic Predisposition to Disease.
650		2	_aGenetic Variation.
650		2	_aGenome, Human.
830		0	_aHenry Stewart talks. _pBiomedical & life sciences collection. _pCopy number variation.
856	4	0	_uhttps://hstalks.com/bs/1395/
856	4	2	_uhttps://hstalks.com/bs/p/439/ _3Series
999			_c77702 _d77702