Related references
Note: Only part of the references are listed.Spectrum of RB1 mutations identified in 403 retinoblastoma patients
Elizabeth A. Price et al.
JOURNAL OF MEDICAL GENETICS (2014)
LINE-1 Elements in Structural Variation and Disease
Christine R. Beck et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 12 (2011)
An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous family
L. Samuelov et al.
BRITISH JOURNAL OF DERMATOLOGY (2011)
Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastoma
Vidya Latha Parsam et al.
JOURNAL OF BIOSCIENCES (2011)
The NF1 Gene Contains Hotspots for L1 Endonuclease-Dependent De Novo Insertion
Katharina Wimmer et al.
PLOS GENETICS (2011)
A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma
Vidya Latha Parsam et al.
JOURNAL OF GENETICS (2009)
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
Francois-Olivier Desmet et al.
NUCLEIC ACIDS RESEARCH (2009)
Clustal W and clustal X version 2.0
M. A. Larkin et al.
BIOINFORMATICS (2007)
A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation
Catherine Dehainault et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
RBI gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database -: art. no. 53
JR Valverde et al.
BMC GENETICS (2005)
L1Base: from functional annotation to prediction of active LINE-1 elements
T Penzkofer et al.
NUCLEIC ACIDS RESEARCH (2005)
Hot L1s account for the bulk of retrotransposition in the human population
B Brouha et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications
J Alonso et al.
HUMAN MUTATION (2001)