MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

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Bibliographic Details
Published inHuman mutation Vol. 27; no. 8; pp. 814 - 821
Main Authors Vorstman, J.A.S., Jalali, G.R., Rappaport, E.F., Hacker, A.M., Scott, C., Emanuel, B.S.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.08.2006
Subjects
22q11DS
atypical rearrangements
conotruncal anomaly
DiGeorge
MLPA
VCFS
velocardiofacial syndrome
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Bibliography:Communicated by Paolo Fortina
ArticleID:HUMU20330
Charles E.H. Upham Chair in Pediatrics
This article is a US Government work, and, as such, is in the public domain in the United States of America.
istex:F52660B30B7D57B61B3DEE94EBF06460141EF24B
ark:/67375/WNG-DR22TLSB-W
National Institutes of Health - No. CA 39926; No. DC02027; No. HD26979
ISSN:1059-7794
1098-1004
DOI:10.1002/humu.20330