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

doi:10.1111/cge.13364

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 journal › Letter › peer-review

Original language	English
Pages (from-to)	386-388
Number of pages	3
Journal	Clinical Genetics
Volume	94
Issue number	3-4
DOIs	https://doi.org/10.1111/cge.13364
Publication status	Published - Oct 1 2018

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1111/cge.13364

Cite this

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

author = "R. Ricotti and T. Nardo and P. Striano and M. Stefanini and D. Orioli and E. Botta",

year = "2018",

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volume = "94",

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journal = "Clinical Genetics",

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AU - Striano, P.

AU - Stefanini, M.

AU - Orioli, D.

AU - Botta, E.

PY - 2018/10/1

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DO - 10.1111/cge.13364

M3 - Letter

AN - SCOPUS:85046796920

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SP - 386

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JO - Clinical Genetics

JF - Clinical Genetics

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