Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.Novel MSH2 splice-site mutation in a young patient with Lynch syndrome.Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression
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Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 29 January 2017
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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type
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Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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Novel Implications in Molecular Diagnosis of Lynch Syndrome.
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P2860
P356
P1476
Novel Implications in Molecular Diagnosis of Lynch Syndrome
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P2093
Paola Izzo
Raffaella Liccardo
P2860
P304
P356
10.1155/2017/2595098
P577
2017-01-29T00:00:00Z