Recurrent polytopic chromaffin paragangliomas in a 9-year-old boy resulting from a novel germline mutation in the von Hippel-Lindau gene. [electronic resource]
Producer: 20020604Description: 145-8 p. digitalISSN:- 1077-4114
- Abdominal Neoplasms -- genetics
- Amino Acid Substitution
- Child
- Codon -- genetics
- Diagnosis, Differential
- Humans
- Hypertension -- etiology
- Ligases -- genetics
- Magnetic Resonance Imaging
- Male
- Mutation, Missense
- Neuroblastoma -- diagnosis
- Paraganglioma, Extra-Adrenal -- genetics
- Point Mutation
- Seizures -- etiology
- Thoracic Neoplasms -- genetics
- Tumor Suppressor Proteins
- Ubiquitin-Protein Ligases
- Von Hippel-Lindau Tumor Suppressor Protein
- von Hippel-Lindau Disease -- diagnosis
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Publication Type: Case Reports; Journal Article
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