Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Mefford HC; Sharp AJ; Baker C; Itsara A; Jiang Z; Buysse K; Huang S; Maloney VK; Crolla JA; Baralle D; Collins A; Mercer C; Norga K; de Ravel T; Devriendt K; Bongers EM; de Leeuw N; Reardon W; Gimelli S; Bena F; Hennekam RC; Male A; Gaunt L; Clayton-Smith J; Simonic I; Park SM; Mehta SG; Nik-Zainal S; Woods CG; Firth HV; Parkin G; Fichera M; Reitano S; Lo Giudice M; Li KE; Casuga I; Broomer A; Conrad B; Schwerzmann M; Räber L; Gallati S; Striano P; Coppola A; Tolmie JL; Tobias ES; Lilley C; Armengol L; Spysschaert Y; Verloo P; De Coene A; Goossens L; Mortier G; Speleman F; van Binsbergen E; Nelen MR; Hochstenbach R; Poot M; Gallagher L; Gill M; McClellan J; King MC; Regan R; Skinner C; Stevenson RE; Antonarakis SE; Chen C; Estivill X; Menten B; Gimelli G; Gribble S; Schwartz S; Sutcliffe JS; Walsh T; Knight SJ; Sebat J; Romano C; Schwartz CE; Veltman JA; de Vries BB; Vermeesch JR; Barber JC; Willatt L; Tassabehji M; Eichler EE; The New England Journal Of Medicine, 2008, vol. 359, issue 16, p 1685, ISSN 15334406. ISBN 15334406.
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