000			02087ngm a2200373 a 4500
001			HST2180_1_2
003			UkLoHST
006			m c
007			cr|cna|||a||||
007			vz|czazum
008			080121s2009 enk|||||||||||s|||v|eng d
028	5	0	_a2180 _bHenry Stewart Talks
035			_a(UkLoHST)1404
035			_a(UkLU-K)001155584
040			_aUkLU-K _beng _cUkLU-K
100	1		_aBeaudet, Arthur L. _4spk
245	1	4	_aThe case for offering all women amniocentesis and chromosomal microarray analysis _h[electronic resource] / _cArthur L. Beaudet.
260			_aLondon : _bHenry Stewart Talks, _c2009.
300			_a1 online resource (1 streaming video file (35 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: Array-based copy number analysis (ABCNA) -- Chromosomal microarray analysis (CMA) -- CMA methodology -- Targeted patient population -- Detection of clinically significant abnormalities -- Copy number variation -- CMA vs. karyotype -- Prenatal use of arrays -- Microarray genetic screening -- Search and destroy concern and eugenics -- Tests which should be abandoned -- Prenatal CMA clinical protocol -- Array-CGH -- Findings of uncertain significance -- Recent cases -- Interpreting uncertain array data -- Advantages of amino and array analysis -- Two kinds of uncertainty -- Non-paternity concerns -- Study design.
506			_aAccess restricted to subscribers.
538			_aMode of access: World Wide Web.
650		2	_aAmniocentesis.
650		2	_aGene Dosage.
650		2	_aGenetic Variation.
650		2	_aOligonucleotide Array Sequence Analysis.
650		2	_aWomen's Health.
830		0	_aHenry Stewart talks. _pBiomedical & life sciences collection. _pCopy number variation.
856	4	0	_uhttps://hstalks.com/bs/1404/
856	4	2	_uhttps://hstalks.com/bs/p/439/ _3Series
999			_c77694 _d77694