Deletion (1)(p32.2­p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: a new microdeletion syndrome?

Mulatinho, Milene; Llerena Junior, Juan Clinton; Leren, Trond P.; Rao, P. Nagesh; Quintero-Rivera, Fabiola.
Artículo en Inglés | ARCA | ID: arc-10650

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