Article
Deletion (1)(p32.2–p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: a new microdeletion syndrome?
Fecha
2008Registro en:
MULATINHO, Milene et al. Deletion (1)(p32.2–p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: a new microdeletion syndrome? American Journal of Medical Genetics Part A, v. 146A, n. 17, p. 2284-2290, 2008.
1552-4825
10.1002/ajmg.a.32454
Autor
Mulatinho, Milene
Llerena Junior, Juan Clinton
Leren, Trond P.
Rao, P. Nagesh
Quintero-Rivera, Fabiola