1. Baldini, Rossella, Mascaro, Martina, Meroni, Germana. 2020. The MID1 gene product in physiology and disease. In Gene, 747, 144655. doi:10.1016/j.gene.2020.144655. https://pubmed.ncbi.nlm.nih.gov/32283114/
2. Winter, Jennifer, Basilicata, M Felicia, Stemmler, Marc P, Krauss, Sybille. 2016. The MID1 protein is a central player during development and in disease. In Frontiers in bioscience (Landmark edition), 21, 664-82. doi:. https://pubmed.ncbi.nlm.nih.gov/26709798/
3. De Falco, Francesca, Cainarca, Silvia, Andolfi, Grazia, Franco, Brunella, Meroni, Germana. . X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum. In American journal of medical genetics. Part A, 120A, 222-8. doi:. https://pubmed.ncbi.nlm.nih.gov/12833403/
4. Micale, Lucia, Russo, Federica, Mascaro, Martina, Meroni, Germana, Castori, Marco. 2022. Opitz syndrome: improving clinical interpretation of intronic variants in MID1 gene. In Pediatric research, 93, 1208-1215. doi:10.1038/s41390-022-02237-y. https://pubmed.ncbi.nlm.nih.gov/35953512/
5. Qiao, Yingying, Zhou, Yuan, Song, Chao, Zhang, Xin, Zou, Yi. . MID1 and MID2 regulate cell migration and epithelial-mesenchymal transition via modulating Wnt/β-catenin signaling. In Annals of translational medicine, 8, 1021. doi:10.21037/atm-20-5583. https://pubmed.ncbi.nlm.nih.gov/32953821/