TY  - GEN
AU  - Cortés M,Fanny
AU  - Alliende R,M Angélica
AU  - Barrios R,Andrés
AU  - Curotto L,Bianca
AU  - Santa María V,Lorena
AU  - Barraza O,Ximena
AU  - Troncoso A,Ledia
AU  - Mellado S,Cecilia
AU  - Pardo V,Rosa
TI  - [Clinical, genetic and molecular features in 45 patients with Prader-Willi syndrome]
SN  - 0034-9887
PY  - 2005///1215
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chile
KW  - Female
KW  - Gene Deletion
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Methylation
KW  - Phenotype
KW  - Prader-Willi Syndrome
KW  - diagnosis
KW  - Retrospective Studies
N1  - Publication Type: English Abstract; Journal Article
UR  - https://doi.org/10.4067/s0034-98872005000100005
ER  -