Showing items 1 - 2 of 2

Integration of EpiSign, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re-classification of an ARID1B missense variant

- Forwood, Caitlin, Ashton, Katie, Katf, Hala, Riveros, Carlos, Hsieh, Tzung-Chien, Krawitz, Peter, Robinson, Peter N., Dudding-Byth, Tracy, Sadikovic, Bekim, Pinner, Jason, Buckley, Michael F., Roscioli, Tony, Zhu, Ying, Zhang, Futao, Dias, Kerith-Rae, Standen, Krystle, Evans, Carey-Anne, Carey, Louise, Cardamone, Michael, Shalhoub, Carolyn

Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome

- Dagar, Vinod, Hutchison, Wendy, Muscat, Andrea, Krishnan, Anita, Hoke, David, Buckle, Ashley, Siswara, Priscillia, Amor, David J., Mann, Jeffrey, Pinner, Jason, Colley, Alison, Wilson, Meredith, Sachdev, Rani, McGillivray, George, Edwards, Matthew, Kirk, Edwin, Collins, Felicity, Jones, Kristi, Taylor, Juliet, Hayes, Ian, Dudding-Byth, Tracey

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