Disorders

VHL-Related Pheochromocytoma

Gene	Locus	Protein
VHL	3p25.3	Von Hippel-Lindau disease tumor suppressor

Laboratory	Test Method	Prenatal	Carrier *
Cliniques universitaires Saint Luc, Center for Human Genetics - Brussels, Belgium	• Sequence analysis of the entire coding region
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany	• Sequence analysis of the entire coding region
Mayo Clinic - Minnesota, Endocrine Laboratory - Rochester, MN, USA	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain	• Sequence analysis of the entire coding region
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands	• Sequence analysis of the entire coding region • Deletion/duplication analysis
Royal Devon and Exeter Hospital, Department of Molecular Genetics - Exeter, Great Britain	• Sequence analysis of the entire coding region

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.