Associated Papers
From musk to body odor: Decoding olfaction through genetic variation.
Li B et al.
Plos Genetics, 2022
35113854 (PubMed )
Supplement: pgen.1009564.s008.xlsx › Sheet1
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
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