Wadey, R., Mckie, J., Papapetrou, C., Sutherland, H., Lohman, F., Osinga, J., et al. (1999). Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]. AMERICAN JOURNAL OF HUMAN GENETICS, 65(1), 247-249 [10.1086/302468].

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

AMATI, FRANCESCA;NOVELLI, GIUSEPPE;
1999-01-01

Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/03 - Genetica Medica
English
Con Impact Factor ISI
DiGeorge Syndrome; Gene Deletion; Genetic Testing; Humans; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Proteins; Chromosomes, Human, Pair 22
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1378096/
Wadey, R., Mckie, J., Papapetrou, C., Sutherland, H., Lohman, F., Osinga, J., et al. (1999). Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]. AMERICAN JOURNAL OF HUMAN GENETICS, 65(1), 247-249 [10.1086/302468].
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
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/117974
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