Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
KBG syndrome
OMIM:148050
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
07/22/2015
PubMed IDs:
30088855 27667800 23494856 28250421 28449295 25464108 27900361 25652421 23184435 21782149 25838844 30877071 29224748
Assertion Criteria:
Submitter Submitted Date:
09/11/2023

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