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Items: 9

1.

Differences in the levels of UV repair and in clinical symptoms in two sibs affected by xeroderma pigmentosum.

Stefanini M, Keijzer W, Dalprà L, Elli R, Porro MN, Nicoletti B, Nuzzo F.

Hum Genet. 1980;54(2):177-82.

PMID:
7390491
2.

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.

Broughton BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JH, Botta E, Stefanini M, King MD, Weber CA, Cole J, et al.

Am J Hum Genet. 1995 Jan;56(1):167-74. Review.

4.

Xeroderma pigmentosum.

Norgauer J, Idzko M, Panther E, Hellstern O, Herouy Y.

Eur J Dermatol. 2003 Jan-Feb;13(1):4-9. Review.

PMID:
12609773
5.

Xeroderma pigmentosum group D patient bearing lentigo maligna without neurological symptoms.

Fukuro S, Yamaguchi J, Mamada A, Kondo S, Satoh Y.

Dermatologica. 1990;181(2):129-33. Review.

PMID:
2242781
6.

Replication of damaged DNA: molecular defect in xeroderma pigmentosum variant cells.

Cordonnier AM, Fuchs RP.

Mutat Res. 1999 Oct 22;435(2):111-9. Review.

PMID:
10556591
7.

Xeroderma pigmentosum.

Der Kaloustian VM, Kurban AK.

Br J Dermatol. 1973 May;88(5):513-5. Review. No abstract available.

PMID:
4577062
8.

Genetics and skin cancer of xeroderma pigmentosum in Japan.

Takebe H, Nishigori C, Satoh Y.

Jpn J Cancer Res. 1987 Nov;78(11):1135-43. Review. No abstract available.

PMID:
3121549
9.

[Importance and heterogenity of xeroderma pigmentosum syndrome].

Jung EG.

Hautarzt. 1973 May;24(5):175-9. Review. German. No abstract available.

PMID:
4584914

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