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Q51939769-CDD822A8-3168-446C-A0B0-83701BEC8E5F
Q51939769-CDD822A8-3168-446C-A0B0-83701BEC8E5F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51939769-CDD822A8-3168-446C-A0B0-83701BEC8E5F
Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3.
P2860
Q51939769-CDD822A8-3168-446C-A0B0-83701BEC8E5F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51939769-CDD822A8-3168-446C-A0B0-83701BEC8E5F
rank
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type
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wasDerivedFrom
abfcc08493e985402c86524dd0061298d936257b
P2860
SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.