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28 August 2001
The pVHL-associated SCF ubiquitin ligase complex: Molecular genetic analysis of elongin B and C, Rbx1 and HIF-1α in renal cell carcinoma
Oncogene 20 , 5067–5074

Rights & permissionsfor article The pVHL-associated SCF ubiquitin ligase complex: Molecular genetic analysis of elongin B and C, Rbx1 and HIF-1α in renal cell carcinoma . Opens in a new window.
2 October 2003
Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma
- Mark R Morris
- , Luke B Hesson
- , Kate J Wagner
- , Neil V Morgan
- , Dewi Astuti
- , Robert D Lees
- , Wendy N Cooper
- , JouAnn Lee
- , Dean Gentle
- , Fiona Macdonald
- , Takeshi Kishida
- , Richard Grundy
- , Masahiro Yao
- , Farida Latif
- & Eamonn R Maher
Oncogene 22 , 6794–6801

Rights & permissionsfor article Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma . Opens in a new window.
11 July 2012
Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility
European Journal of Human Genetics 21 , 347–351

Rights & permissionsfor article Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility . Opens in a new window.
15 November 2001
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours
- Dewi Astuti
- , Angelo Agathanggelou
- , Sofia Honorio
- , Ashraf Dallol
- , Tommy Martinsson
- , Per Kogner
- , Carole Cummins
- , Hartmut PH Neumann
- , Raimo Voutilainen
- , Patricia Dahia
- , Charis Eng
- , Eamonn R Maher
- & Farida Latif
Oncogene 20 , 7573–7577

Rights & permissionsfor article RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours . Opens in a new window.
Research | 5 February 2012
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility
- Dewi Astuti
- , Mark R Morris
- , Wendy N Cooper
- , Raymond H J Staals
- , Naomi C Wake
- , Graham A Fews
- , Harmeet Gill
- , Dean Gentle
- , Salwati Shuib
- , Christopher J Ricketts
- , Trevor Cole
- , Anthonie J van Essen
- , Richard A van Lingen
- , Giovanni Neri
- , John M Opitz
- , Patrick Rump
- , Irene Stolte-Dijkstra
- , Ferenc Müller
- , Ger J M Pruijn
- , Farida Latif
- & Eamonn R Maher
Nature Genetics 44 , 277–284

Rights & permissionsfor article Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility . Opens in a new window.

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The pVHL-associated SCF ubiquitin ligase complex: Molecular genetic analysis of elongin B and C, Rbx1 and HIF-1α in renal cell carcinoma

Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma

Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility

RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

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