Next Article in Journal
Loss-of-Function Variants in EFEMP1 Cause a Recognizable Connective Tissue Disorder Characterized by Cutis Laxa and Multiple Herniations
Next Article in Special Issue
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome
Previous Article in Journal
Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
Previous Article in Special Issue
Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome
 
 
Article

Article Versions Notes

Action Date Notes Link
article xml file uploaded 30 March 2021 14:01 CEST Original file -
article xml uploaded. 30 March 2021 14:01 CEST Update -
article pdf uploaded. 30 March 2021 14:01 CEST Version of Record https://www.mdpi.com/2073-4425/12/4/509/pdf-vor
article supplementary file uploaded. 30 March 2021 14:01 CEST - https://www.mdpi.com/2073-4425/12/4/509#supplementary
article html file updated 30 March 2021 14:02 CEST Original file -
article xml file uploaded 1 April 2021 02:54 CEST Update -
article xml uploaded. 1 April 2021 02:54 CEST Update -
article pdf uploaded. 1 April 2021 02:54 CEST Updated version of record https://www.mdpi.com/2073-4425/12/4/509/pdf-vor
article html file updated 1 April 2021 02:56 CEST Update -
article xml file uploaded 2 April 2021 11:03 CEST Update -
article xml uploaded. 2 April 2021 11:03 CEST Update https://www.mdpi.com/2073-4425/12/4/509/xml
article pdf uploaded. 2 April 2021 11:03 CEST Updated version of record https://www.mdpi.com/2073-4425/12/4/509/pdf
article html file updated 2 April 2021 11:04 CEST Update -
article html file updated 10 April 2021 12:55 CEST Update -
article html file updated 3 August 2021 16:46 CEST Update -
article html file updated 25 July 2022 09:57 CEST Update https://www.mdpi.com/2073-4425/12/4/509/html
Back to TopTop