Bibliographic Details
| Title: |
Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype. |
| Authors: |
Stagi S; Health's Sciences Department, University of Florence, Anna Meyer Children's University Hospital, Florence, Italy. stefano.stagi@yahoo.it., Lapi E, Pantaleo M, Chiarelli F, Seminara S, de Martino M |
| Source: |
BMC medical genetics [BMC Med Genet] 2014 Jan 30; Vol. 15, pp. 16. Date of Electronic Publication: 2014 Jan 30. |
| Publication Type: |
Case Reports; Journal Article |
| Journal Info: |
Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350 (Electronic) Linking ISSN: 14712350 NLM ISO Abbreviation: BMC Med Genet Subsets: MEDLINE |
| Database: |
MEDLINE Ultimate |
