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)

Access to Document

10.1111/cge.13364

Cite this

@article{e339a0320561448f91d5a49113111762,

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",

month = oct,

day = "1",

doi = "10.1111/cge.13364",

language = "English",

volume = "94",

pages = "386--388",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "3-4",

}

TY - JOUR

T1 - Phenotypic variability in xeroderma pigmentosum group G

T2 - An uncommon case with severe prenatal-onset Cockayne syndrome features

AU - Ricotti, R.

AU - Nardo, T.

AU - Striano, P.

AU - Stefanini, M.

AU - Orioli, D.

AU - Botta, E.

PY - 2018/10/1

Y1 - 2018/10/1

UR - http://www.scopus.com/inward/record.url?scp=85046796920&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85046796920&partnerID=8YFLogxK

U2 - 10.1111/cge.13364

DO - 10.1111/cge.13364

M3 - Letter

AN - SCOPUS:85046796920

VL - 94

SP - 386

EP - 388

JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 3-4

ER -

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

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this