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Xu, JX, Kilpatrick, N, Baker, NL, Penington, A, Farlie, PG, Tan, TY.
Clinical and Molecular Characterisation of Children with Pierre Robin Sequence and Additional Anomalies..
Mol Syndromol
7(6)
:
322 -328
2016
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Yap, P, Super, L, Qin, J, Burgess, T, Prodanovic, Z, Edwards, C, Thomas, R, Carpenter, K, Tan, TY.
Congenital Retroperitoneal Teratoma in Neurofibromatosis Type 1..
Pediatr Blood Cancer
63(4)
:
706 -708
2016
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Cheah, K, Au, T, Wynn, S, Tan, T, Yip, R, Chan, D.
Genetic Control of Hypertrophic Chondrocyte to Osteoblast Differentiation in Development and Skeletal Disorders.
The FASEB Journal
30(S1)
:
2016
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Bennett, JT, Tan, TY, Alcantara, D, Tétrault, M, Timms, AE, Jensen, D, Collins, S, Nowaczyk, MJM, Lindhurst, MJ, Christensen, KM, et al.
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis..
Am J Hum Genet
98(3)
:
579 -587
2016
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Paul, JL, Pope-Couston, R, Wake, S, Burgess, T, Tan, TY.
Communicating microarray results of uncertain clinical significance in consultation summary letters and implications for practice..
Eur J Hum Genet
25(1)
:
22 -30
2016
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