Abstract
Disorders caused by a defect in a single gene follow the patterns of inheritance described by Mendel. Individual disorders of this type are often rare but are important because they are numerous (3000-4000 single gene traits have been listed). Risks within an affected family are usually high and are calculated by knowing the mode of inheritance and details of the family pedigree.
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CITATION STYLE
APA
Kingston, H. M. (1989). ABC of clinical genetics. Mendelian inheritance. BMJ, 298(6670), 375–378. https://doi.org/10.1136/bmj.298.6670.375
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