Suchergebnisse - "Defferrari, Raffaella"

1

Detection of MYCN amplification and chromosome 1p36 loss in neuroblastoma by cDNA microarray comparative genomic hybridization

von: Scaruffi, Paola

2004, in: Molecular diagnosis & therapy

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2

Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients

von: Mandich, Paola

1995, in: Journal of neurology

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3

Constitutional 11q14-q22 chromosome deletion syndrome in a child with neuroblastoma MYCN single copy

von: Passariello, Annalisa

2013transfer abstract, in: Edge minimization in de Bruijn graphs

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