Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features

R. Ricotti, T. Nardo, P. Striano, M. Stefanini, D. Orioli, E. Botta

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)386-388
Number of pages3
JournalClinical Genetics
Issue number3-4
Publication statusPublished - Oct 1 2018

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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