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Molecular investigations, Communication, Informed consent, Documents, Genetic, Laboratory, Set of forms
Now Panorama® offers screening for twin and egg donor pregnancies! Panorama® is the first Non Invasive DNA screen for fetal chromosomal abnormalities providing: Zigosity information; Individual fetal fractions […]
Molecular investigations, Prenatal diagnosis, Genetic, Natera, Next Generation Sequencing, NIPT, Non Invasive Prenatal Testing, Panorama, Test DNA fetale, Test prenatale su sangue materno
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 collaborators a constant […]
Molecular investigations, Communication, Genetic, Laboratory, Quality
Discover our new gene panels and the application of the NGS technique in Microgenomics: Hemihypertrophia panel Hipopituitarism & GH Deficit panel Klippel-Feil Syndrome panel Non […]
Molecular investigations, Postnatal diagnosis, Genetic, Human Genetics, Laboratory, Next Generation Sequencing, NGS, NGS panel
We wish to inform that during christmas period Microgenomics laboratory will be OPENED. As every holiday period, please be warned about all samples shipment requests through our express courier service, […]
Consulting services, Christmas time, Communication, Holidays, Schedule
Microgenomics staff is working for you! Discover our new gene panels and the application of the NGS technique in Microgenomics: OPTIC ATROPHY panel OVERGROWTH SYNDROMES […]
Molecular investigations, Atrofie ottiche, Genetic, Laboratory, Next Generation Sequencing, NGS, Obesity, Sindromi da overgrowth
During the summer we will be OPENED. Single closing day Monday, August 14th. We wish to inform that Microgenomics laboratory will be OPENED for all August […]
Microgenomics laboratory announces the introduction of a new line of NGS genetic tests dedicated to oncology diagnostics. Every day in Italy will find nearly 1,000 […]
Molecular investigations, Tumor, Oncology diagnostic, Genetic, Human genetics laboratory, Myeloid Leukemia, Next Generation Sequencing, NGS, Oncology, Hereditary cancer