Journal
Genetics in Medicine
Publication Date
3-1-2024
Volume
26
Issue
3
First Page
101035
Document Type
Open Access Publication
DOI
10.1016/j.gim.2023.101035
Rights and Permissions
Chopra M, Savatt JM, Bingaman TI, Good ME, Morgan A, Cooney C, Rossel AM, VanHoute B, Cordova I, Mahida S, Lanzotti V, Baldridge D, Gurnett CA, Piven J, Hazlett H, Pomeroy SL, Sahin M, Payne PRO, Riggs ER, Constantino JN; Brain Gene Registry Consortium. Clinical variants paired with phenotype: A rich resource for brain gene curation. Genet Med. 2024 Mar;26(3):101035. doi: 10.1016/j.gim.2023.101035. © 2023 The Authors. Published by Elsevier Inc. on behalf of American College of Medical Genetics and Genomics. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Recommended Citation
Chopra, Maya; Lanzotti, Virginia; Baldridge, Dustin; Gurnett, Christina A; Payne, Philip R O; and et al., "Clinical variants paired with phenotype: A rich resource for brain gene curation." Genetics in Medicine. 26, 3. 101035 (2024).
https://digitalcommons.wustl.edu/oa_4/4537
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
