000			02094nam a2200361 a 4500
001			ebr10671288
003			CaPaEBR
006			m u
007			cr cn|||||||||
008			110502s2012 nyua sb 001 0 eng d
010			_z 2011018627
020			_z9781613248669 (hardcover)
020			_z9781614700272 (e-book)
040			_aCaPaEBR _cCaPaEBR
035			_a(OCoLC)847626729
050	1	4	_aRB155.6 _b.G4613 2012eb
082	0	4	_a616/.042 _223
245	0	0	_aGenetic diagnoses _h[electronic resource] / _cRadha Jonnalagedda Sarma, editor.
260			_aHauppauge, N.Y. : _bNova Science Publishers, _cc2012.
300			_axi, 202 p. : _bill.
490	1		_aGenetics - research and issues
500			_a"Nova biomedical."
504			_aIncludes bibliographical references and index.
505	0		_aDefining a cause : result priority between preeclampsia and thyroid function / Ioannis Katsakoulas, Clio P. Mavragani -- Molecular diagnosis of thalassemia / Wen Wang, Boran Jiang, Samuel S. Chong -- Fuzzy logic and the least squares method in diagnosis problem solving / Alexander P. Rotshtein, Hanna B. Rakytyanska -- Molecular diagnosis of spinocerbellar ataxias / Laia Rodriguez-Revenga ... [et al.] -- Genetics of left ventricular noncompaction / Radha J. Sarma -- A genetic diagnosis to type 1 diabetes / Jose Luis Santiago, Laura Espino-Paisan, Elena Urcelay -- State of the heart on genetics of congential heart diseases : molecular basis, genetic diagnosis, and counselling / Giuseppe Limongelli ... [et al.].
533			_aElectronic reproduction. _bPalo Alto, Calif. : _cebrary, _d2013. _nAvailable via World Wide Web. _nAccess may be limited to ebrary affiliated libraries.
650		0	_aHuman chromosome abnormalities _xDiagnosis.
650		0	_aMolecular biology.
655		7	_aElectronic books. _2local
700	1		_aSarma, Radha Jonnalagedda.
710	2		_aebrary, Inc.
830		0	_aGenetics--research and issues series.
856	4	0	_uhttp://site.ebrary.com/lib/rucke/Doc?id=10671288 _zAn electronic book accessible through the World Wide Web; click to view
999			_c62405 _d62405