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Article

A case of de novo mosaic 18q21.3 deletion with a mild phenotype.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2014

Alp M Y, Cebi A H, Seyhan S, Cansu A, Ikbal M

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Share to Child, Preschool
Share to Chromosome Deletion
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Share to Chromosomes, Human, Pair 18

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 24783659

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