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Commentary on "Investigations of somatic NKX2-5 mutations in congenital heart disease (CHD)"

 
: Reamon-Buettner, S.M.; Borlak, J.

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Journal of medical genetics (2010), Published Online July 9, 2010, 2 pp.
ISSN: 0022-2593
English
Journal Article, Electronic Publication
Fraunhofer ITEM ()
base sequence; cohort studies; DNA mutational analysis; congenital heart defect; molecular sequence data; single nucleotide polymorphism; Transcription factors; mutation

: http://publica.fraunhofer.de/documents/N-150000.html