Results 1 -
3
of
3
for
apert
- Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure of the bones of the ...
- ... the FGFR2 gene have been found to cause Apert syndrome. This condition causes premature closure of the ... symptoms.More than 98 percent of cases of Apert syndrome are caused by one of two mutations ...
- ... Becchetti A, Carinci P, Baroni T, Bodo M. Apert and Crouzon syndromes: clinical findings, genes and extracellular ...