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Volumn 41, Issue 1, 2003, Pages E3-
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Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene
a a |
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Author keywords
[No Author keywords available]
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Indexed keywords
GLYCINE;
LIGASE;
SERINE;
TUMOR SUPPRESSOR PROTEIN;
UBIQUITIN PROTEIN LIGASE;
VHL PROTEIN, HUMAN;
VON HIPPEL LINDAU PROTEIN;
ADRENAL TUMOR;
AMINO ACID SUBSTITUTION;
BILATERAL HEARING LOSS;
CASE REPORT;
CHILD;
CRYPTORCHISM;
DEVELOPMENTAL DISORDER;
GENETICS;
GERMLINE MUTATION;
HUMAN;
MALE;
MICROCEPHALY;
MISSENSE MUTATION;
MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A;
PHEOCHROMOCYTOMA;
SYNDROME;
TUMOR SUPPRESSOR GENE;
VON HIPPEL LINDAU DISEASE;
ADRENAL GLAND NEOPLASMS;
AMINO ACID SUBSTITUTION;
CHILD;
CRYPTORCHIDISM;
DEVELOPMENTAL DISABILITIES;
GENES, TUMOR SUPPRESSOR;
GERM-LINE MUTATION;
GLYCINE;
HEARING LOSS, BILATERAL;
HUMANS;
LIGASES;
MALE;
MICROCEPHALY;
MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A;
MUTATION, MISSENSE;
PHEOCHROMOCYTOMA;
SERINE;
SYNDROME;
TUMOR SUPPRESSOR PROTEINS;
UBIQUITIN-PROTEIN LIGASES;
VON HIPPEL-LINDAU DISEASE;
VON HIPPEL-LINDAU TUMOR SUPPRESSOR PROTEIN;
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EID: 0037208695
PISSN: None
EISSN: 15236838
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (5)
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References (0)
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