Associated Papers
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Ogata T et al.
Plos One, 2014
24637876 (PubMed )
Supplement: pone.0091598.s004.pdf
Assessing the emerging oncogene protein kinase C epsilon as a candidate gene in families with Carney complex-2.
Toledo RA et al.
Clinical Endocrinology, 2012
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