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Q35644285-C2CCB9FE-9588-4736-A19E-8419AE12E3DE
Q35644285-C2CCB9FE-9588-4736-A19E-8419AE12E3DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35644285-C2CCB9FE-9588-4736-A19E-8419AE12E3DE
An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene
P407
Q35644285-C2CCB9FE-9588-4736-A19E-8419AE12E3DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35644285-C2CCB9FE-9588-4736-A19E-8419AE12E3DE
rank
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type
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Statement
P407
English