Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]

Autor:	Wadey, R, Mckie, J, Papapetrou, C, Sutherland, H, Lohman, F, Osinga, J, Frohn, I, Hofstra, R, Meijers, C, Amati, F, Conti, E, Pizzuti, A, Dallapiccola, B, Novelli, G, Scambler, P
Jazyk:	angličtina
Rok vydání:	1999
Předmět:	DiGeorge Syndrome Gene Deletion Genetic Testing Humans Polymorphism Genetic Polymorphism Single-Stranded Conformational Proteins Chromosomes Human Pair 22 Genetic Settore MED/03 - Genetica Medica Single-Stranded Conformational Polymorphism Pair 22 Chromosomes Human
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=od______3667::2d71fd1e4584f27db0daa698871042ab http://hdl.handle.net/2108/117974 Zobrazit plný text záznamu