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Fig. 4 | BMC Medical Genetics

Fig. 4

From: Intronic mutation of the VHL gene associated with central nervous system hemangioblastomas in two Chinese families with Von Hippel–Lindau disease: case report

Fig. 4

Family tree of the patients with c.464-1G > C point mutation. Three-generation pedigree of the patient family showing that the synonymous VHL variant c.464-1G > C segregates with affected family members. The number on the upper left corner of each patient with VHL-associated HGBs indicates the age of each operation for CNS HGBs

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BMC Medical Genetics

ISSN: 1471-2350

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