Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis
Abstract Background Craniosynostosis is one of the major genetic disorders affecting 1 in 2,100–2,500 live newborn children. Environmental and genetic factors are involved in the manifestation of this disease. The suggested genetic causes of craniosynostosis are pathogenic variants in FGFR1, FGFR2,...
|Main Authors:||, , , , , ,|
|Series:||Molecular Genetics & Genomic Medicine|