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Q36083125-F0B0B5A5-01A3-4365-BE0A-75688EE65063
Q36083125-F0B0B5A5-01A3-4365-BE0A-75688EE65063
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36083125-F0B0B5A5-01A3-4365-BE0A-75688EE65063
Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148
P2860
Q36083125-F0B0B5A5-01A3-4365-BE0A-75688EE65063
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36083125-F0B0B5A5-01A3-4365-BE0A-75688EE65063
rank
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type
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Statement
wasDerivedFrom
5176cddd82eca0b9925cc5271f4c50f9d6a736ae
P2860
A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.