Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
anophthalmia/microphthalmia-esophageal atresia syndrome
Microphthalmia, syndromic 3
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
08/27/2023
PubMed IDs:
15240551 16283891 16470798 16651659 16892470 16932809 17219395 17522144 18285410 18385794 18831064 19921648 22382802 24033328 24498598 24804704 29335358 34562068 35170016 36602867
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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