Molecular genetic analysis of von Hippel–Lindau disease

Author:

Richards 1,Webster 2,Mcmahon 3,Woodward 4,Rose 5,Maher 1

Affiliation:

1. Division of Medical and Molecular Genetics, University of Birmingham Department of Paediatrics and Child Health, The Medical School, Birmingham;

2. Department of Ophthalmology

3. Molecular Genetics Laboratory, Addenbrooke's Hospital, Cambridge;

4. Cambridge University Department of Pathology, Cambridge;

5. Regional Molecular Genetics Laboratory, Birmingham Women's Hospital, Birmingham, UK

Publisher

Wiley

Subject

Internal Medicine

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3. Exploring the role of defective fibronectin matrix assembly in the VHL-associated CNS hemangioblastoma;Drug Metabolism and Personalized Therapy;2018-09-25

4. Von Hippel-Lindau Disease;Atlas of Genetic Diagnosis and Counseling;2017

5. Endolymphatic Sac Tumor;Diagnostic Pathology: Head and Neck;2016

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