Abstract
Autism spectrum disorders (ASDs) are phenotypically as well as genetically heterogeneous developmental disorders with a strong heritability. Clinical and basic science research has described many replicated genetic risk factors. Many findings can well be translated into clinical human genetic practice. The current article summarizes results of genetic studies in ASD, provides a diagnostic algorithm for the clinical human genetic work-up reflecting the German health care system options and gives information with regard to the obligatory genetic counselling after a clinical genetic assessment.
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Freitag, C. M., Haslinger, D., Yousaf, A., & Waltes, R. (2020). Clinical genetic testing and counselling in autism spectrum disorder. Medizinische Genetik, 32(1), 31–37. https://doi.org/10.1515/medgen-2020-2001
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