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Exclusion of inv(2)(p16.1;q14.3) as the cause of a severe congenital disease by Next-Generation Sequencing
Exclusion of inv(2)(p16.1;q14.3) as the cause of a severe congenital disease by Next-Generation Sequencing
2015
Manuela Pinto Cardoso
Michael E. Talkowski
João Freixo
Rui Gonçalves
Cynthia C. Morton
Dezső David
Keywords:
DNA sequencing
Cancer research
Disease
Biology
Pediatrics
congenital disease
Medicine
Correction
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