Next Article in Journal
A Method for Detecting and Analyzing Facial Features of People with Drug Use Disorders
Next Article in Special Issue
When Familial Hearing Loss Means Genetic Heterogeneity: A Model Case Report
Previous Article in Journal
Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome
Previous Article in Special Issue
Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Prader–Willi Syndrome
 
 
Case Report

Article Versions Notes

Diagnostics 2021, 11(9), 1561; https://doi.org/10.3390/diagnostics11091561
Action Date Notes Link
article xml file uploaded 28 August 2021 12:42 CEST Original file -
article xml uploaded. 28 August 2021 12:42 CEST Update -
article pdf uploaded. 28 August 2021 12:42 CEST Version of Record https://www.mdpi.com/2075-4418/11/9/1561/pdf-vor
article supplementary file uploaded. 28 August 2021 12:42 CEST - https://www.mdpi.com/2075-4418/11/9/1561#supplementary
article html file updated 28 August 2021 12:44 CEST Original file -
article xml file uploaded 1 September 2021 16:44 CEST Update -
article xml uploaded. 1 September 2021 16:44 CEST Update https://www.mdpi.com/2075-4418/11/9/1561/xml
article pdf uploaded. 1 September 2021 16:44 CEST Updated version of record https://www.mdpi.com/2075-4418/11/9/1561/pdf
article html file updated 1 September 2021 16:45 CEST Update -
article html file updated 30 July 2022 03:12 CEST Update https://www.mdpi.com/2075-4418/11/9/1561/html
Back to TopTop