Work

Impact of molecular mechanisms, including deletion size, on Prader–Willi syndrome phenotype: study of 75 patients

Year: 2004

Type: article

Study design: Observational Study

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2005.00377.x

Authors: MC Varela, F Kok, N Setian, CA Kim, CP Koiffmann

Institutions: Universidade de São Paulo, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Fundação de Amparo à Pesquisa do Estado de São Paulo

OpenAlex ID: W1578646984

FWCI: 2.478

Cites: 28

Cited by: 120

Related to: 10