Work

Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment

Year: 2003

Type: article

Study design: Case Report

Source: European Journal of Human Genetics

DOI: 10.1038/sj.ejhg.5200907

Authors: Britt-Marie Anderlid, Jacqueline Schoumans, Åsa Hallqvist, Ylva Ståhl, Agneta Wallin, Elisabeth Blennow, Magnus Nordenskjöld

Institutions: Karolinska University Hospital, Karolinska Institutet, Danderyds sjukhus, S:t Eriks Ögonsjukhus

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Medical Research Council

OpenAlex ID: W2043919690

FWCI: 2.466

Cites: 19

Cited by: 46

Related to: 10