Work

Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping

Year: 1999

Type: article

Study design: Case Report

Source: Prenatal Diagnosis

DOI: 10.1002/(sici)1097-0223(199912)19:12<1143::aid-pd730>3.3.co;2-0

Authors: B. Peschka, J. Leygraaf, D. Hansmann, M. Hansmann, E. Schröck, T. Ried, H. Engels, G. Schwanitz, R. Schubert

Institutions: University of Bonn, National Institutes of Health, National Human Genome Research Institute

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

OpenAlex ID: W4252135145

FWCI: 0.529

Cites: 22

Cited by: 21

Related to: 10