(Q69932448)
Statements
A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11-12 and on an atypical PWS patient with apparently normal karyotype (English)
Kamei T
Hamabe JI
Matsumoto T
Abe K
Harada N
Ishikiriyama S
Hasegawa T
Miyazaki K
Mizuno S