The power of homozygosity mapping: discovery of new genetic defects in patients with retinal dystrophy

Autor:	Littink, K.W., Hollander, A.I. den, Cremers, F.P., Collin, R.W.J.
Rok vydání:	2012
Předmět:	Genetics and epigenetic pathways of disease [NCMLS 6] Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6]
Zdroj:	Advances in Experimental Medicine and Biology, 723, 345-51 Advances in Experimental Medicine and Biology, 723, pp. 345-51
ISSN:	0065-2598
Popis:	Item does not contain fulltext
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9862d6480095271ea7c684baf76229dc http://hdl.handle.net/2066/109901 Zobrazit plný text záznamu