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From: Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study

Original Submission
3 Sep 2023 Submitted Original manuscript
4 Dec 2023 Reviewed Reviewer Report - Lavinia di Meglio
11 Dec 2023 Reviewed Reviewer Report - fabiana interlandi
19 Dec 2023 Author responded Author comments - Hailong Huang
Resubmission - Version 2
19 Dec 2023 Submitted Manuscript version 2
Publishing
22 Dec 2023 Editorially accepted
3 Jan 2024 Article published 10.1186/s12884-023-06223-y

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