Work

Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells

Year: 1992

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/1.5.307

Authors: Thomas Ried, Greg Landes, William Dackowski, Katherine Klinger, David C. Ward

Institutions: Yale University, Sequenom (United States)

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

Funders: Deutsche Forschungsgemeinschaft, National Institutes of Health, National Human Genome Research Institute

Awards: G2263828082, NEW METHODS FOR ANALYZING HUMAN GENES &THEIR DEFECTS, G722564751, HIGH RESOLUTION GENE MAPPING BY IN SITU HYBRIDIZATION

OpenAlex ID: W2169513241

FWCI: 6.55

Cites:

Cited by: 116

Related to: 10