Center for Human Genetics and Laboratory Diagnostics (AHC) Martinsried
Our diagnostic expertise covers the analysis of body fluids and tissue samples with molecular genetic, cytogenetic, flow cytomteric and biochemical techniques. Our molecular diagnostics portfolio comprises the whole spectrum of advanced technologies such as multi-gene panel sequencing (MGPS), clinical exome sequencing (CES), whole Exome sequencing (WES) and RNA sequencing. Other applications of next generation sequencing (NGS) include HLA typing and the Prenatalis® non-invasive prenatal test (NIPT). We also employ several array platforms such as AffymetrixTM, AgilentTM or Illumina iScanTM to perform array CGH, SNP array analyses and methylation profiles. Other important methods include flow cytometry (FACS scan) and tandem mass spectrometry.
Our highly qualified medical, scientific and technical staff offers comprehensive and individual support services for physicians regarding all clinical and diagnostic questions. Our patient´s services include genetic counselling for developmental delay in children, rare diseases and prenatal testing in München, Martinsried, Augsburg and Kempten, as well as infertility counselling and immunization consultations .
Our office hours are Monday to Friday from 08:00 am to 06:00 pm (UTC + 1, summer time + 2), except of national and regional holidays.
Central Office Phone: +49-89-895578-0
Our vision is the translation of current scientific knowledge in genome research into clinically useful diagnostic approaches. Therefore, we maintain colaborations with clinical and scientific institutions at national and international universities and participate actively in several research projects. We offer seminars and symposia for physicians, scientists and the technical staff on a regular basis to share our current knowledge and its impact on diagnostic medicine. Please feel always welcome to one of our next events.