Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome.
Le Meur N, Goldenberg A, Michel-Adde C, Drouin-Garraud V, Blaysat G, Marret S, Amara SA, Moirot H, Joly-Hélas G, Mace B, Kleinfinger P, Saugier-Veber P, Frébourg T, Rossi A.
Le Meur N, et al. Among authors: blaysat g.
Am J Med Genet A. 2005 May 1;134(4):439-42. doi: 10.1002/ajmg.a.30660.
Am J Med Genet A. 2005.
PMID: 15810003