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Author/Creator Tang, Dave

1. A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number‐dependent manner. Issue 4 (31st January 2020)

Authors:
Bertuzzi, Maria; Tang, Dave; Calligaris, Raffaella; Vlachouli, Christina; Finaurini, Sara; Sanges, Remo; Goldwurm, Stefano; Catalan, Mauro; Antonutti, Lucia; Manganotti, Paolo; Pizzolato, Gilberto; Pezzoli, Gianni; Persichetti, Francesca; Carninci, Piero; Gustincich, Stefano
Journal:
Human mutation
Issue:
Volume 41:Issue 4(2020)
Page Start:
807
Record Type:
Journal Article
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2. Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population. (9th March 2021)

Authors:
Jamieson, Sarra E; Fakiola, Michaela; Tang, Dave; Scaman, Elizabeth; Syn, Genevieve; Francis, Richard W; Coates, Harvey L; Anderson, Denise; Lassmann, Timo; Cordell, Heather J; Blackwell, Jenefer M
Journal:
Clinical infectious diseases
Issue:
Volume 73:Number 10(2021)
Page Start:
1860
Record Type:
Journal Article
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3. High expression of insulin receptor on tumour‐associated blood vessels in invasive bladder cancer predicts poor overall and progression‐free survival. Issue 2 (3rd May 2017)

Authors:
Roudnicky, Filip; Dieterich, Lothar C; Poyet, Cedric; Buser, Lorenz; Wild, Peter; Tang, Dave; Camenzind, Peter; Ho, Chien Hsien; Otto, Vivianne I; Detmar, Michael
Journal:
Journal of pathology
Issue:
Volume 242:Issue 2(2017)
Page Start:
193
Record Type:
Journal Article
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5. Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene. (December 2017)

Authors:
Abraham, Mary; Li, Dong; Tang, Dave; O'Connell, Susan; McKenzie, Fiona; Lim, Ee; Hakonarson, Hakon; Levine, Michael; Choong, Catherine
Journal:
International journal of pediatric endocrinology
Issue:
Volume 2017(2017)
Page Start:
1
Record Type:
Journal Article
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6. The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service. Issue 1 (December 2016)

Authors:
Baynam, Gareth; Pachter, Nicholas; McKenzie, Fiona; Townshend, Sharon; Slee, Jennie; Kiraly-Borri, Cathy; Vasudevan, Anand; Hawkins, Anne; Broley, Stephanie; Schofield, Lyn; Verhoef, Hedwig; Walker, Caroline; Molster, Caron; Blackwell, Jenefer; Jamieson, Sarra; Tang, Dave; Lassmann, Timo; Mina, K...
Journal:
Orphanet journal of rare diseases
Issue:
Volume 11:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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