Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
osteogenesis imperfecta type 1
OMIM:166200
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
07/22/2015
PubMed IDs:
1988452 9067755 2037280 9295084 3403550 8950680 2295701 7816518 8100209 12538651 8723681 3082886 2309707 2913053 1770532 15728585 21834035 11286507 15024692 2511192 8364588 8757037 8910493 8456809 7789952 2794057 18409203 8097422 8786074 1737847 3667599 1613761 2298750 3108247 1864604 7881420 8408653 2500431 1634225 1874719 2339700
Assertion Criteria:
Submitter Submitted Date:
09/11/2023

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