Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
Cowden syndrome 1
OMIM:158350
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
10/31/2023
PubMed IDs:
10400993 10910075 11755638 12928488 12938083 15254063 15589575 17392703 17768394 18972196 19847259 20565722 21194675 21303970 21430697 21659347 22252256 23335809 23934601 24136893 26678657 26798346 27890237 28526761 30287823 31216739 32923874 8673088 9345101 9467011
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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