AB085. Imprinting mutation of CDKN1C in Beckwith-Wiedemann Syndrome: inheritance, genetic counselling and surveillance

Hui Bein Chew, Winnie Peitee Ong, Muzhirah Aisha Md Haniffa, Huey Yin Leong, Thurga Krishnan, Rozaida Yuen Ying Poh, Meow Keong Thong, Mohd Taufik Ishak, Wee Teik Keng