Autosomal Dominant Punnett Square Achondroplasia
July 16, 2024
SOLVED: Achondroplasia is a common form of dwarfism caused by autosomal dominant mutation in the fibroblast growth factor receptor 3 (Fgfr3) gene. If a person with achondroplasia (Aa) married and had children Can a healthy woman and her husband who suffers from dwarfism have a normal child? The first and only child was born with the same disability and they plan to have more Achondroplasia: Domiant Trait - YouTube Autosomal Dominant Punnett Square Achondroplasia
![Patterns of Disease Inheritance - almostadoctor]("https://almostadoctor.co.uk/sites/all/files/image/Systems/Paeds/Genetics/Punnetts%20Square.png"){kind=link}
