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TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia
Ogata T,
Niihori T,
Tanaka N,
Kawai M,
Nagashima T,
et al.
(2014)
TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia.
PLOS ONE 9(3): e91598.
https://doi.org/10.1371/journal.pone.0091598