Associated Papers
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35768426 (PubMed )
Supplement: 41531_2022_346_MOESM2_ESM.xlsx › SupTab1
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
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Supplement: pone.0091598.s006.pdf
Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines.
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