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AB085. Imprinting mutation of CDKN1C in Beckwith-Wiedemann Syndrome: inheritance, genetic counselling and surveillance
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@article{{ATM}{7590}, author = {Chew, H., Ong, W., Haniffa, M., Leong, H., Krishnan, T., Poh, R., Thong, M., Ishak, M., Keng, W.}, title = {AB085. Imprinting mutation of CDKN1C in Beckwith-Wiedemann Syndrome: inheritance, genetic counselling and surveillance}, journal = {Annals of Translational Medicine}, volume = {3}, number = {Suppl 2}, year = {2015}, url = {https://atm.amegroups.org/article/view/7590} }