lifesciences
Innopsys

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 100 consecutive clinical cases

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 100 consecutive clinical cases

F. Fiorentino1, Fiorina Caiazzo1, Stefania Napolitano1, Letizia Spizzichino1, Sara Bono1,Mariateresa Sessa1, Andrea Nuccitelli1, Anil Biricik1, Anthony Gordon2, Giuseppe Rizzo1 and Marina Baldi1  
1. ‘GENOMA'—Molecular Genetics Laboratory, Via PO, 102, 00198 Rome, Italy 
2. Bluegnome Ltd, Cambridge CB22 5LD, UK 

Abstract

Objective: To assess the feasibility of offering array-based comparative genomic hybridization testing for prenatal diagnosis as a first-line test, a prospective study was performed, comparing the results achieved from array comparative genomic hybridization (aCGH) with those obtained from conventional karyotype.

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