Associated Papers
Missense variants in homeobox domain of PBX1 cause coracoclavicular ankylosis.
Iwai M et al.
European Journal of Human Genetics : Ejhg, 2026
41162587 (PubMed )
Supplement: 41431_2025_1973_MOESM1_ESM.pdf
Whole-exome sequencing and bioinformatics analysis of a case of non-alpha-fetoprotein-elevated lung hepatoid adenocarcinoma.
Yao Y et al.
Frontiers in Pharmacology, 2022
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