Article ISI SCOPUS
Circulation: Cardiovascular Genetics  (2017)

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the &ITGPR98&IT Locus on 5q14.3

Repetto, GM; McGinn, DMM; Campbell, CL; Blonska, A; Bassett, AS; Chow, EWC; Mlynarski, EE; Devriendt K.; Carmel, M; Michaelovsky, E; Antonarakis, SE; Coleman, K; Tomita-Mitchell, A; Mitchell, ME; Digilio, MC; et. al.

Keywords: chromosomes, genotype, digeorge syndrome, tetralogy of fallot, ivelo-cardio-facial syndrome

Más información

Título según WOS: Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the &ITGPR98&IT Locus on 5q14.3
Título según SCOPUS: Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3
Título de la Revista: Circulation: Cardiovascular Genetics
Volumen: 10
Número: 5
Editorial: Lippincott Williams and Wilkins
Fecha de publicación: 2017
Idioma: English
DOI:

10.1161/CIRCGENETICS.116.001690
Notas: ISI, SCOPUS