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Results: 6

1.

Identification of PATCHED mutations in medulloblastomas by direct sequencing.

Dong J, Gailani MR, Pomeroy SL, Reardon D, Bale AE.

Hum Mutat. 2000 Jul;16(1):89-90.

PMID:
10874314
[PubMed - indexed for MEDLINE]
2.

PTCH mutations: distribution and analyses.

Lindström E, Shimokawa T, Toftgård R, Zaphiropoulos PG.

Hum Mutat. 2006 Mar;27(3):215-9. Review.

PMID:
16419085
[PubMed - indexed for MEDLINE]
3.

[Clinical and genetic study in 22 patients with basal cell nevus syndrome].

Pruvost-Balland C, Gorry P, Boutet N, Magnaldo T, Mamelle G, Margulis A, Kolb F, Duvillard P, Spatz A, Brugières L, Chompret A, Avril MF.

Ann Dermatol Venereol. 2006 Feb;133(2):117-23. Review. French.

PMID:
16508594
[PubMed - indexed for MEDLINE]
4.

A mouse model for medulloblastoma and basal cell nevus syndrome.

Corcoran RB, Scott MP.

J Neurooncol. 2001 Jul;53(3):307-18. Review.

PMID:
11718263
[PubMed - indexed for MEDLINE]
5.

[From gene to disease: basal cell naevus syndrome].

de Meij TG, Baars MJ, Gille JJ, Hack WW, Haasnoot K, van Hagen JM.

Ned Tijdschr Geneeskd. 2005 Jan 8;149(2):78-81. Review. Dutch.

PMID:
15688838
[PubMed - indexed for MEDLINE]
6.

Medulloblastoma biology in the post-genomic era.

Archer TC, Pomeroy SL.

Future Oncol. 2012 Dec;8(12):1597-604. doi: 10.2217/fon.12.151. Review.

PMID:
23231521
[PubMed - indexed for MEDLINE]
Free PMC Article

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