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Detection of single clone deletions using array CGH: identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system.
Tokuyasu, Taku A; Cotter, Philip D; Segraves, Richard; Harris, Jeffrey; Elder, Melissa E; Gonzales, Marcos; Pinkel, Daniel; Albertson, Donna G; Rauen, Katherine A.
Affiliation
  • Tokuyasu TA; Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA 94115, USA.
Am J Med Genet A ; 143A(9): 925-32, 2007 May 01.
Article in En | MEDLINE | ID: mdl-17394204
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Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 22 / Chromosome Deletion / DiGeorge Syndrome / Nucleic Acid Hybridization Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2007 Document type: Article Affiliation country: Estados Unidos
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 22 / Chromosome Deletion / DiGeorge Syndrome / Nucleic Acid Hybridization Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2007 Document type: Article Affiliation country: Estados Unidos