Comprehensive genetic diagnosis of non-syndromic hereditary hearing loss by targeted resequencing of 32 genes with use of Hapolpex desingn and IonTorrent PGM seqencer

Number of the records: 1

Title	Comprehensive genetic diagnosis of non-syndromic hereditary hearing loss by targeted resequencing of 32 genes with use of Hapolpex desingn and IonTorrent PGM seqencer
Author	Nagyová Emília
Co-authors	Dvorská D.
	Szemes Tomáš
	Kádaši Ľudevít 1952- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV ^ORCID
	Minárik G.

Source document	European Journal of Human Genetics. Vol. 22, Supplement 1 (2014), p. 81
Language	eng - English
Note	Abstract. - ITMS 26240220067
Document kind	rozpis článkov z periodík (rbx)
Category	AEGA - Abstracts of scientific papers published in foreign impacted journals registered in Current Contents Connect
Category of document (from 2022)	V3 - Vedecký výstup publikačnej činnosti z časopisu
Type of document	abstrakt
Year	2014

article

rok	CC	IF	IF Q (best)	JCR Av Jour IF Perc	SJR	SJR Q (best)	CiteScore
	A

rok vydania	rok metriky	IF	IF Q (best)	SJR	SJR Q (best)
2014	2013	4.225	Q1	1.914	Q1

Number of the records: 1