Nuova mutazione del gene NIPBL in paziente affetto da Sindrome di Cornelia de Lange: report clinico e correlazione genotipo-fenotipo

6533b86cfe1ef96bd12c8620

RESEARCH PRODUCT

Nuova mutazione del gene NIPBL in paziente affetto da Sindrome di Cornelia de Lange: report clinico e correlazione genotipo-fenotipo

Davide Vecchio V. Antona Mario Giuffre E. Salzano L. Lagalla E. Pisaneschi A. Selicorni Giovanni Corsello

subject

gene NIPBL Sindrome Cornelia de Lange Settore MED/38 - Pediatria Generale E Specialistica

description

gene NIPBL, Sindrome Cornelia de Lange

year	journal	country	edition	language
2016-01-01

http://hdl.handle.net/10447/211328

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