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Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype

PaperCitations, authors & open-access status

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype is a paper indexed in PICO Portal from OpenAlex.

How many citations does Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype have?

PICO Portalcitation count

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype has 563 citations in the OpenAlex counts PICO Portal stores.

When was Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype published?

PICO Portalyear

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype has 1995 year in the PICO Portal index.

What is the open-access status of Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype?

PICO Portaloa status

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype has closed oa status in the PICO Portal index.

What is the DOI of Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype?

PICO Portaldoi

The DOI for Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype is on the source record.

What is the PMID of Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype?

PICO Portalpmid

The PMID for Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype is on the source record.

What is the OpenAlex record for Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype?

PICO Portalopenalex

The OpenAlex for Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype is on the source record.

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