Physician geneticists Lars-Erik Wehner

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The services specified above (Human genome, interdisciplinary science, Prevention of hereditary diseases, Therapy of hereditary diseases, medical diagnostics, u.a.) might be restricted or unavailable.

Human genetics is an interdisciplinary science that combines medical diagnostics with molecular biological research and methodology. Physician geneticists usually study human chromosomes by fluorescence microscopy to study sets of chromosomes for specific conditions or syndromes.

Part of human genetics is medical genetics, which deals with the diagnosis and treatment of hereditary diseases. These include eg sickle cell anemia, cystic fibrosis and Huntington's disease.

Physician geneticists are concerned with the genome of humans. There are Hereditary diseases, such as cystic fibrosis, sickle cell anemia or Huntington's disease. The basis for the work of the physician geneticists is the federal law on gene diagnostics.

With the aid of fluorescence microscopy, human chromosome records are examined to find out syndromes, syndromes and the like.