Source:http://linkedlifedata.com/resource/pubmed/id/11155407
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2001-1-11
|
pubmed:abstractText |
To determine the efficacy of multicolor fluorescent in situ hybridization (M-FISH), which paints each chromosome in a unique color, for identification of congenital derivative and marker chromosomes. MATERIAL, METHODS AND CASES: Commercially available M-FISH probes were used to label each chromosome in a specific fluorescent color. Six representative cases involving derivative chromosomes, markers, and subtle anomalies were analyzed by M-FISH.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0025-6196
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
76
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
16-21
|
pubmed:dateRevised |
2007-10-29
|
pubmed:meshHeading |
pubmed-meshheading:11155407-Adult,
pubmed-meshheading:11155407-Child,
pubmed-meshheading:11155407-Chromosome Aberrations,
pubmed-meshheading:11155407-Chromosome Disorders,
pubmed-meshheading:11155407-Chromosome Painting,
pubmed-meshheading:11155407-Female,
pubmed-meshheading:11155407-Humans,
pubmed-meshheading:11155407-Infant, Newborn,
pubmed-meshheading:11155407-Male,
pubmed-meshheading:11155407-Mutation,
pubmed-meshheading:11155407-Nucleic Acid Probes,
pubmed-meshheading:11155407-Telomere
|
pubmed:year |
2001
|
pubmed:articleTitle |
Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders.
|
pubmed:affiliation |
Division of Laboratory Genetics, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA. sjalal@mayo.edu
|
pubmed:publicationType |
Journal Article,
Case Reports
|