Open AccessAB058. Prader-Willi syndrome: clinical and genetic features
Author(s) -
Lan An Thuy
Publication year - 2017
Publication title -
annals of translational medicine
Language(s) - English
Resource type - Journals
eISSN - 2305-5847
pISSN - 2305-5839
DOI - 10.21037/atm.2017.s058
Subject(s) - hypotonia , short stature , medicine , phenotype , genetic disorder , genomic imprinting , pediatrics , obesity , genetic syndromes , genetics , bioinformatics , gene , endocrinology , biology , gene expression , dna methylation
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