Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
osteogenesis imperfecta type 3
OMIM:259420
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
06/08/2023
PubMed IDs:
10417276 11286507 15024692 1634225 1737847 1988452 2037280 21834035 21912751 2295701 2298750 2309707 2402497 2500431 2745420 2794057 2913053 3108247 3170557 3198624 3244312 3403550 3722186 4031065 6469997 7789952 7942841 8097422 8408653 8723681 8757937 9007315 9067755 9295084 9443882
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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