Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
OMIM:615485
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
07/22/2015
PubMed IDs:
29305346 23383720 29445472 29367179 31638014 29316359 24044690 28100473 27075689 27901041 28955728 31180560 32240826
Assertion Criteria:
Submitter Submitted Date:
09/11/2023

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