uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets.
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology.
Show others and affiliations
2004 (English)In: Int J Mol Med, ISSN 1107-3756, Vol. 13, no 2, 273-9 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 13, no 2, 273-9 p.
Keyword [en]
Chromosomes; Human; Pair 22, Expressed Sequence Tags, Female, Gene Dosage, Humans, Male, Nucleic Acid Hybridization, Oligonucleotide Array Sequence Analysis, Polymerase Chain Reaction, Research Support; Non-U.S. Gov't, Research Support; U.S. Gov't; Non-P.H.S., Sequence Deletion
Identifiers
URN: urn:nbn:se:uu:diva-71961PubMedID: 14719134OAI: oai:DiVA.org:uu-71961DiVA: diva2:99872
Available from: 2005-05-16 Created: 2005-05-16 Last updated: 2011-01-12

Open Access in DiVA

No full text

Other links

PubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=14719134&dopt=Citation
By organisation
Department of Genetics and Pathology

Search outside of DiVA

GoogleGoogle Scholar

pubmed
urn-nbn

Altmetric score

pubmed
urn-nbn
Total: 345 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf