A clinical case of identical twins with hypogonadotropic hypogonadism,
primary empty sella syndrome and identified rare CHD7 gene variant
- Sava Petrov
, - Ekaterina Babadzhanova,
- Maria Orbetzova,
- Hristo Ivanov
05 Mar 2023Submitted to Clinical Case Reports 07 Mar 2023Submission Checks Completed
07 Mar 2023Assigned to Editor
09 Mar 2023Reviewer(s) Assigned
10 Mar 2023Review(s) Completed, Editorial Evaluation Pending
22 Mar 2023Editorial Decision: Revise Minor
29 Mar 20231st Revision Received
05 Apr 2023Submission Checks Completed
05 Apr 2023Assigned to Editor
05 Apr 2023Review(s) Completed, Editorial Evaluation Pending
17 Apr 2023Reviewer(s) Assigned
02 May 2023Editorial Decision: Revise Minor
03 May 20232nd Revision Received
11 May 2023Submission Checks Completed
11 May 2023Assigned to Editor
11 May 2023Review(s) Completed, Editorial Evaluation Pending
22 May 2023Editorial Decision: Accept
