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Q52621434-156316E4-D2B1-40E6-8345-124E182F8C54
Q52621434-156316E4-D2B1-40E6-8345-124E182F8C54
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Statement
http://www.wikidata.org/entity/statement/Q52621434-156316E4-D2B1-40E6-8345-124E182F8C54
Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome).
P2860
Q52621434-156316E4-D2B1-40E6-8345-124E182F8C54
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52621434-156316E4-D2B1-40E6-8345-124E182F8C54
rank
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Statement
wasDerivedFrom
2227a00858b54a35d1a4a1c73025b1710aa27b0e
P2860
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndrome.