Work

The Familial Lentiginosis Syndromes are Emerging from the Obscurity Imposed by Rarity: New Genes and Genetic Loci for Multiple Tumors and Developmental Defects*

Year: 1998

Type: article

Source: Hormone and Metabolic Research

DOI: 10.1055/s-2007-978885

Author: C. Stratakis

Institutions: National Institutes of Health, Georgetown University, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Language: English

Topic: Genetic and rare skin diseases.

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2042281572

FWCI: 1.167

Cites:

Cited by: 11

Related to: 10