Purpose: Smith-Magenis syndrome (SMS) is a complex disorder that includes mental retardation, craniofacial and skeletal ... SMS300 showed a heterozygous deletion of four bases, GCCG, starting ...
1p36 Deletion Syndrome (1p36DS) is a genetic condition ... including distinct craniofacial features, developmental delays, hypotonia (reduced muscle tone), epilepsy, and various heart defects.
一些您可能无法访问的结果已被隐去。
显示无法访问的结果