RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients

Charlotte J Dommering; Berber M Mol; Annette C Moll; Margaret Burton; Jacqueline Cloos; Josephine C Dorsman; Hanne Meijers-Heijboer; Annemarie H van der Hout

doi:10.1136/jmedgenet-2014-102264

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Cancer genetics

Original article

RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients

Authors

Charlotte J Dommering Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands PubMed articles Google scholar articles
Berber M Mol Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands PubMed articles Google scholar articles
Annette C Moll Department of Ophthalmology, VU University Medical Center, Amsterdam, The Netherlands PubMed articles Google scholar articles
Margaret Burton Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands PubMed articles Google scholar articles
Jacqueline Cloos Department of Hematology, VU University Medical Center, Amsterdam, The Netherlands Department of Pediatric Oncology/Hematology, VU University Medical Center, Amsterdam, The Netherlands PubMed articles Google scholar articles
Josephine C Dorsman Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands PubMed articles Google scholar articles
Hanne Meijers-Heijboer Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands PubMed articles Google scholar articles
Annemarie H van der Hout Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands PubMed articles Google scholar articles

Correspondence to Charlotte J Dommering, Department of Clinical Genetics, VU University Medical Center, PO Box 7057, Amsterdam 1007 MB, The Netherlands; cj.dommering{at}vumc.nl

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Citation

Dommering CJ, Mol BM, Moll AC, et al

RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients

Journal of Medical Genetics 2014;51:366-374.

Publication history

Received January 2, 2014
Accepted February 26, 2014
First published March 31, 2014.

Online issue publication

April 27, 2016

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