From clinical features to molecular defects: lack of clear genotype-phenotype relationships in Cockayne syndrome. (Comunicazione a convegno)

Type

• Prodotto della ricerca (Classe)
• Comunicazione a convegno (Classe)

Label

• From clinical features to molecular defects: lack of clear genotype-phenotype relationships in Cockayne syndrome. (Comunicazione a convegno) (literal)

Anno

• 2004-01-01T00:00:00+01:00 (literal)

Alternative label

• Stefanini M., Oneda R., Nardo T., Colella S., Negrini S., Botta E., Lehmann A.R., Fawcett H., Mallery D (2004)
  From clinical features to molecular defects: lack of clear genotype-phenotype relationships in Cockayne syndrome.
  in Cockayne syndrome and related disorders of DNA repair and transcription: from bench to bedside and back, Lansdowne, VA, USA
  (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

• Stefanini M., Oneda R., Nardo T., Colella S., Negrini S., Botta E., Lehmann A.R., Fawcett H., Mallery D (literal)

Titolo

• From clinical features to molecular defects: lack of clear genotype-phenotype relationships in Cockayne syndrome. (literal)

Prodotto di

• Institute of molecular genetics (IGM) (Istituto)

Autore CNR

• ELENA BOTTA (Persona)
• MIRIA STEFANINI (Unità di personale interno)

Incoming links:

Prodotto

• Institute of molecular genetics (IGM) (Istituto)

Autore CNR di

• ELENA BOTTA (Persona)
• MIRIA STEFANINI (Unità di personale interno)