IMG_20150327_12411q copia home - diagnosi prenatale copia Test genetici Intolleranze alimentari home - studio segregazione home-qualità-1000x400

Quality

Microgenomics has obtained the ISO 9001 and SIGU Certification.  Since its birth Microgenomics has dedicated its activity to continuous improvement…

Prenatal diagnosis

Prenatal diagnosis consists of investigations, invasive or non-invasive, allowing monitoring of the health of the fetus during pregnancy in order…

(Italiano) Test intolleranze alimentari

Sorry, this entry is only available in Italian.

Familiar segregations

Establishing the source of genomic alterations is important to define the pathogenetic significance and to determine more accurately the risk…

Research & Development

The Research and Development division formulates multidisciplinary projects: the objective is the implementation of new diagnostic methods, the optimization of…

Advanced Genomic Solutions

intro servizi

Services

Microgenomics is a genetic testing laboratory which arose with the aim of creating a highly specialized diagnostics centre in order to provide molecular investigations based on microarray technology for the study and diagnosis of genetic diseases. Specialists…

More »
IMG_20150327_12411q copia

Quality

Microgenomics has obtained the ISO 9001 and SIGU Certification.  Since its birth Microgenomics has dedicated its activity to continuous improvement of quality and services provided. The company has always been committed to convey to its…

More »

Download

Microgenomics Company pays great attention to its customer information requirements. In this section you can find forms, to apply for exams or to send biological samples, detailed brochures and our Public Services Charter.

More »

News from Microgenomics

carrier day

(Italiano) Microgenomics al Career Day 2016

17 May , 2016

Sorry, this entry is only available in Italian.

More »

News from the world

Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene.

8 Feb , 2016

Am J Med Genet. 2016 Jan 11 Authors Ronzoni L, Tagliaferri…

Heterozygous deletion of the LRFN2 gene is associated with working memory deficits.

11 Nov , 2015

Eur J Hum Genet. 2015 Oct 21 Authors Thevenon J, Souchay…