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Q37646069-20B09421-A4AF-4C19-ADDF-27800B6B3554
Q37646069-20B09421-A4AF-4C19-ADDF-27800B6B3554
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http://www.wikidata.org/entity/statement/Q37646069-20B09421-A4AF-4C19-ADDF-27800B6B3554
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.
P2860
Q37646069-20B09421-A4AF-4C19-ADDF-27800B6B3554
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37646069-20B09421-A4AF-4C19-ADDF-27800B6B3554
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wasDerivedFrom
98695456fd0a3cc71913ba9d7e8afa97282f5987
P2860
Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes