Description
prada willi case-study, Prader-Willi syndrome (PWS) is a genetic disorder that occurs as the result of absence of expression of paternal genes from chromosome 15 q11.2-q13. The clinical features .
Beige and white GG Supreme canvas
prader willi syndrome case study
Gold-toned hardware
prader willi syndrome ethiopia
Double G
Inside: 8 open pocket
Chain top handle with 7″ drop
Top zip closure
5.7″W x 3.8″H x 2.5″D
Weight: 0.2lbs approximately