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Q28709034-CDD3CFCC-5933-4E20-8E61-822090A16A18
Q28709034-CDD3CFCC-5933-4E20-8E61-822090A16A18
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http://www.wikidata.org/entity/statement/Q28709034-CDD3CFCC-5933-4E20-8E61-822090A16A18
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
P2860
Q28709034-CDD3CFCC-5933-4E20-8E61-822090A16A18
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28709034-CDD3CFCC-5933-4E20-8E61-822090A16A18
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3882b21374922d02c8d0cd576749d9a290b8ddd1
P2860
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.