rdf:type |
|
lifeskim:mentions |
umls-concept:C0020792,
umls-concept:C0032105,
umls-concept:C0036667,
umls-concept:C0162326,
umls-concept:C0312418,
umls-concept:C0332161,
umls-concept:C0439660,
umls-concept:C0521457,
umls-concept:C1707689,
umls-concept:C1709016,
umls-concept:C1710236,
umls-concept:C1858460
|
pubmed:issue |
7
|
pubmed:dateCreated |
2009-7-6
|
pubmed:abstractText |
The identification of very low-levels of minority sequences has interesting clinical and diagnostic applications. Among these, non-invasive prenatal diagnosis of genetic diseases on fetal DNA circulating in maternal plasma is an emerging field of application.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1434-6621
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
47
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
818-23
|
pubmed:meshHeading |
pubmed-meshheading:19496735-Cystic Fibrosis,
pubmed-meshheading:19496735-DNA,
pubmed-meshheading:19496735-Female,
pubmed-meshheading:19496735-Fetus,
pubmed-meshheading:19496735-Fluorescent Dyes,
pubmed-meshheading:19496735-Genetic Diseases, Inborn,
pubmed-meshheading:19496735-Genotype,
pubmed-meshheading:19496735-Humans,
pubmed-meshheading:19496735-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:19496735-Polymorphism, Single Nucleotide,
pubmed-meshheading:19496735-Pregnancy,
pubmed-meshheading:19496735-Prenatal Diagnosis,
pubmed-meshheading:19496735-Substrate Specificity
|
pubmed:year |
2009
|
pubmed:articleTitle |
High-sensitive microarray substrates specifically designed to improve sensitivity for the identification of fetal paternally inherited sequences in maternal plasma.
|
pubmed:affiliation |
Genomic Unit for the Diagnosis of Human Pathologies, Center for Genomics, Bioinformatics and Biostatistics, San Raffaele Scientific Institute, Milan, Italy.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|