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Complete uniparental disomy of chromosome 1
  • Violet Wallerstein,
  • Leon Grant,
  • Robert Wallerstein
Violet Wallerstein
Drew University

Corresponding Author:vwallerstein@drew.edu

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Leon Grant
Sutter Medical Center Sacramento
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Robert Wallerstein
Laboratory Corporation of America Integrated Genetics
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Abstract

Complete uniparental disomy of chromosome 1 (UPD1) is an uncommon genetic finding about which a specific phenotype has not yet been established. We present a boy who has complete paternal UPD1 and isolated developmental delay. We suggest that there is no clear phenotype of UPD1.

Peer review status:ACCEPTED

16 Sep 2021Submitted to Clinical Case Reports
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22 Sep 2021Submission Checks Completed
22 Sep 2021Assigned to Editor
04 Nov 2021Reviewer(s) Assigned
07 Nov 2021Review(s) Completed, Editorial Evaluation Pending
09 Dec 2021Editorial Decision: Revise Minor
14 Feb 20221st Revision Received
16 Feb 2022Submission Checks Completed
16 Feb 2022Assigned to Editor
16 Feb 2022Review(s) Completed, Editorial Evaluation Pending
07 Mar 2022Editorial Decision: Accept