Work

Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence.

Year: 2000

Type: article

Study design: Case Report

Source: PubMed

Authors: T Lukusa, J P Fryns

Institutions: UCLouvain, KU Leuven

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

OpenAlex ID: W190901752

FWCI: 0.637

Cites:

Cited by: 20

Related to: 10