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. 2011 Mar;19(3).

doi: 10.1038/ejhg.2010.200. Epub 2010 Dec 8.

Clinical utility gene card for: retinoblastoma

Dietmar Lohmann¹, Brenda Gallie, Charlotte Dommering, Marion Gauthier-Villars

Affiliations

Affiliation

¹ Klinische Forschergruppe Ophthalmologische Onkologie und Genetik, Institut für Humangenetik, Universität Duisburg-Essen, Essen, Germany. dietmar.lohmann@uni-due.de

PMID: 21150892
PMCID: PMC3061998
DOI: 10.1038/ejhg.2010.200

Clinical utility gene card for: retinoblastoma

Dietmar Lohmann et al. Eur J Hum Genet. 2011 Mar.

. 2011 Mar;19(3).

doi: 10.1038/ejhg.2010.200. Epub 2010 Dec 8.

Authors

Dietmar Lohmann¹, Brenda Gallie, Charlotte Dommering, Marion Gauthier-Villars

Affiliation

¹ Klinische Forschergruppe Ophthalmologische Onkologie und Genetik, Institut für Humangenetik, Universität Duisburg-Essen, Essen, Germany. dietmar.lohmann@uni-due.de

PMID: 21150892
PMCID: PMC3061998
DOI: 10.1038/ejhg.2010.200

No abstract available

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References

1. Richter S, Vandezande K, Chen N, et al. Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma. Am J Hum Genet. 2003;72:253–269. - PMC - PubMed
1. Lohmann DR, Gallie BL. Retinoblastoma: revisiting the model prototype of inherited cancer. Am J Med Genet C Semin Med Genet. 2004;129:23–28. - PubMed
1. Taylor M, Dehainault C, Desjardins L, et al. Genotype-phenotype correlations in hereditary familial retinoblastoma. Hum Mutat. 2007;28:284–293. - PubMed
1. Noorani HZ, Khan HN, Gallie BL, Detsky AS. Cost comparison of molecular versus conventional screening of relatives at risk for retinoblastoma. Am J Hum Genet. 1996;59:301–307. - PMC - PubMed

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