Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
Shprintzen-Goldberg syndrome
OMIM:182212
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
07/22/2015
PubMed IDs:
8428751 8504310 1631074 7611299 7762551 21594993 18412115 1301946 15032979 15287423 8430317 8040326 8071963 8101042 9101298 8406497 11175294 10766875 17492313 21594992 23103230 23023332 17568394 17366579 11702223 9837823 1569206 8136837 9241263 7633409 20082464 10441597 8281141 20979188 7911051 16333834 1852208
Assertion Criteria:
Submitter Submitted Date:
09/11/2023

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