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Results: 4

1.

Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome.

Mallery DL, Tanganelli B, Colella S, Steingrimsdottir H, van Gool AJ, Troelstra C, Stefanini M, Lehmann AR.

Am J Hum Genet. 1998 Jan;62(1):77-85. Erratum in: Am J Hum Genet 1999 May;64(5):1491.

PMID:
9443879
[PubMed - indexed for MEDLINE]
Free PMC Article
2.
3.

Radiation-induced chromatid aberrations in Cockayne syndrome and xeroderma pigmentosum group C fibroblasts in relation to cancer predisposition.

Price FM, Parshad R, Tarone RE, Sanford KK.

Cancer Genet Cytogenet. 1991 Nov;57(1):1-10.

PMID:
1756475
[PubMed - indexed for MEDLINE]
4.

Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.

Greenhaw GA, Hebert A, Duke-Woodside ME, Butler IJ, Hecht JT, Cleaver JE, Thomas GH, Horton WA.

Am J Hum Genet. 1992 Apr;50(4):677-89.

PMID:
1372469
[PubMed - indexed for MEDLINE]
Free PMC Article

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