Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
chromosome 1p32-p31 deletion syndrome
OMIM:613735
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
07/02/2021
PubMed IDs:
25714559 24462883 27081522 28941020 28452798 22031302 17530927 10518556 30388402 15632069 30388402
Assertion Criteria:
Submitter Submitted Date:
10/27/2022

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