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Q48611267-23DCDF71-CF1E-4FB3-88D4-246105A6E31B
Q48611267-23DCDF71-CF1E-4FB3-88D4-246105A6E31B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48611267-23DCDF71-CF1E-4FB3-88D4-246105A6E31B
Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)].
P2860
Q48611267-23DCDF71-CF1E-4FB3-88D4-246105A6E31B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48611267-23DCDF71-CF1E-4FB3-88D4-246105A6E31B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
86965ecc3f19db55407c55ec50806e60bed6ffb6
P2860
Hypercholesterolemia in children with Smith-Magenis syndrome: del (17) (p11.2p11.2).