MeSH Browser

MeSH Supplementary: Prolactin Deficiency, Isolated
Unique ID: C562708
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562708
Heading Mapped to: *Lactation Disorders; Prolactin / deficiency; *Genetic Diseases, Inborn
Frequency: 10
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Prolactin Deficiency, Isolated MeSH Supplementary Concept Data 2024