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Indian Pediatr ; 2010 Mar; 47(3): 277-279
Article Dans Anglais | IMSEAR | ID: sea-168443

Résumé

A de novo supernumerary marker chromosome (SMC) was identified in a 13- month-old girl who presented with microcephaly and mild mental retardation. On further characterization by oligo-nucleotide array-comparative genomic hybridization [array-CGH], the SMC was confirmed to be 18p.

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