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Q36447391-07EF6136-512F-4401-AE2A-D7EF0268056E
Q36447391-07EF6136-512F-4401-AE2A-D7EF0268056E
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Statement
http://www.wikidata.org/entity/statement/Q36447391-07EF6136-512F-4401-AE2A-D7EF0268056E
Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndrome.
P2860
Q36447391-07EF6136-512F-4401-AE2A-D7EF0268056E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36447391-07EF6136-512F-4401-AE2A-D7EF0268056E
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wasDerivedFrom
1ce5c2d2cdda7be4fa9cf27b886b5e6f4775a6bd
P2860
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome