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Q42672527-B098D4C0-1B9F-4FBF-ADE5-972F0C4D1355
Q42672527-B098D4C0-1B9F-4FBF-ADE5-972F0C4D1355
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http://www.wikidata.org/entity/statement/Q42672527-B098D4C0-1B9F-4FBF-ADE5-972F0C4D1355
Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.
P2860
Q42672527-B098D4C0-1B9F-4FBF-ADE5-972F0C4D1355
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http://www.wikidata.org/entity/statement/Q42672527-B098D4C0-1B9F-4FBF-ADE5-972F0C4D1355
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wasDerivedFrom
f2eb3f2f9de0909254027f116d1e94c3c4480c13
P2860
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.