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Q36594323-B5165697-E3FB-40AC-9D36-658A29F3B1A5
Q36594323-B5165697-E3FB-40AC-9D36-658A29F3B1A5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36594323-B5165697-E3FB-40AC-9D36-658A29F3B1A5
Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome.
P2860
Q36594323-B5165697-E3FB-40AC-9D36-658A29F3B1A5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36594323-B5165697-E3FB-40AC-9D36-658A29F3B1A5
rank
NormalRank
type
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Statement
wasDerivedFrom
55b378ed024d46e6d3e5ef0af346d3a3e6343c4c
P2860
Fourteen-month-old girl with facial skin thinning.