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RB1 homepage - rb1-lsdb - Leiden Open Variation Database

LOVD v.2.0 Build 34 [ Current LOVD status. View all (unique) PubMed references. In the RB1 database. April 26, 2010. October 11, 2017. Submit a sequence variant. Coding DNA reference sequence. For describing sequence variants. Total number of unique DNA variants reported. Total number of individuals with variant(s). Total number of variants reported. Subscribe to updates of this gene. Includes retinoblastoma inducing mutations, innocent variants and all in between. Graphical displays and utilities. Find ...

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RB1 homepage - rb1-lsdb - Leiden Open Variation Database | d-lohmann.de Reviews

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LOVD v.2.0 Build 34 [ Current LOVD status. View all (unique) PubMed references. In the RB1 database. April 26, 2010. October 11, 2017. Submit a sequence variant. Coding DNA reference sequence. For describing sequence variants. Total number of unique DNA variants reported. Total number of individuals with variant(s). Total number of variants reported. Subscribe to updates of this gene. Includes retinoblastoma inducing mutations, innocent variants and all in between. Graphical displays and utilities. Find ...

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1 rb1 lsdb

2 retinoblastoma 1 rb1

3 register as submitter

4 curators dietmar lohmann

5 and larissa novakovic

6 rb1 homepage

7 general information

8 gene name

9 retinoblastoma 1

10 gene symbol

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rb1 lsdb,retinoblastoma 1 rb1,register as submitter,curators dietmar lohmann,and larissa novakovic,rb1 homepage,general information,gene name,retinoblastoma 1,gene symbol,chromosome location,database location,rb1 lovd d lohmann de,curator,dietmar lohmann

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RB1 homepage - rb1-lsdb - Leiden Open Variation Database | d-lohmann.de Reviews

https://d-lohmann.de

LOVD v.2.0 Build 34 [ Current LOVD status. View all (unique) PubMed references. In the RB1 database. April 26, 2010. October 11, 2017. Submit a sequence variant. Coding DNA reference sequence. For describing sequence variants. Total number of unique DNA variants reported. Total number of individuals with variant(s). Total number of variants reported. Subscribe to updates of this gene. Includes retinoblastoma inducing mutations, innocent variants and all in between. Graphical displays and utilities. Find ...

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rb1-lsdb.d-lohmann.de

RB1 homepage - rb1-lsdb - Leiden Open Variation Database

LOVD v.2.0 Build 34 [ Current LOVD status. View all (unique) PubMed references. In the RB1 database. April 26, 2010. May 18, 2015. Submit a sequence variant. Coding DNA reference sequence. For describing sequence variants. Total number of unique DNA variants reported. Total number of individuals with variant(s). Total number of variants reported. Subscribe to updates of this gene. Includes retinoblastoma inducing mutations, innocent variants and all in between. Graphical displays and utilities. Find the ...

rb1-lovd.d-lohmann.de

RB1 homepage - rb1-lsdb - Leiden Open Variation Database

LOVD v.2.0 Build 34 [ Current LOVD status. View all (unique) PubMed references. In the RB1 database. April 26, 2010. May 18, 2015. Submit a sequence variant. Coding DNA reference sequence. For describing sequence variants. Total number of unique DNA variants reported. Total number of individuals with variant(s). Total number of variants reported. Subscribe to updates of this gene. Includes retinoblastoma inducing mutations, innocent variants and all in between. Graphical displays and utilities. Find the ...

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d-lohmann.de

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Index - rb1-lsdb - Leiden Open Variation Database

http://www.d-lohmann.de/docs/index.php

LOVD v.2.0 Build 34 [ Current LOVD status. LOVD manual table of contents. Download the manual as one PDF file. Middot; Installing LOVD. Middot; Before you install. Middot; Download and Extract. Middot; Pre-install Setup. Middot; Install process. Middot; Administrator account details. Middot; Configuring LOVD system settings. Middot; Configuring LOVD modules. Middot; LOVD Setup. Middot; LOVD system settings. Middot; Gene databases. Middot; Creating new genes. Middot; Editing genes. Middot; Emptying genes.

2

Pubmed - rb1-lsdb - Leiden Open Variation Database

http://www.d-lohmann.de/pubmed_references.php

LOVD v.2.0 Build 34 [ Current LOVD status. Ahani et al.(2011) Cancer Genet. 204(6):316-22. Ata-ur-Rasheed et al. (2002) Ophthalmic Genet.(2):121-8. Kubota et al. (1995) Prostate. 1995 Dec;27(6):314-20. Kumaramanickavel et al., (2003), J Genet.82(1-2):39-44. Kumaramanickavel et al. (2003), J Genet.82(1-2):39-44. Miyomoto et al. (1995) Br J Cancer. 1995 Apr;71(4):831-5. Parsam et al. (2009) J Genet. 2009 Dec;88(4):517-27. Parsam et al. (2011) J Biosci. 2011 Jun;36(2):281-7. Bartkova et al., 1996. Braggio e...

3

Register as submitter - rb1-lsdb - Leiden Open Variation Database

http://www.d-lohmann.de/submitters.php?action=register

LOVD v.2.0 Build 34 [ Current LOVD status. Public list of submitters. To register as a new submitter, please fill out the form below. Please note that you do NOT. Need to register to view the data available at these pages. You only need an account for submitting new variants. In addition to your full address, please enter the city for sorting purposes. British Indian Ocean Territory. Cote D'Ivoire (Ivory Coast). Heard and McDonald Islands. Korea (North) (People's Republic). Saint Kitts and Nevis.

4

Submit new data - rb1-lsdb - Leiden Open Variation Database

http://www.d-lohmann.de/submit.php

LOVD v.2.0 Build 34 [ Current LOVD status. To access this area, you need to log in. If you are not registered as a submitter, please do so here. Powered by LOVD v.2.0. 2004-2012 Leiden University Medical Center.

5

Variant listing based on patient origin - rb1-lsdb - Leiden Open Variation Database

http://www.d-lohmann.de/variants_overview_origin.php

LOVD v.2.0 Build 34 [ Current LOVD status. Variant listing based on patient origin. There are no Patient/Origin columns enabled. Therefore this overview is non functional. Powered by LOVD v.2.0. Enabled modules: mutalyzer, recaptcha, showmaxdbid. 2004-2012 Leiden University Medical Center.

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RB1 homepage - rb1-lsdb - Leiden Open Variation Database

LOVD v.2.0 Build 34 [ Current LOVD status. View all (unique) PubMed references. In the RB1 database. April 26, 2010. October 11, 2017. Submit a sequence variant. Coding DNA reference sequence. For describing sequence variants. Total number of unique DNA variants reported. Total number of individuals with variant(s). Total number of variants reported. Subscribe to updates of this gene. Includes retinoblastoma inducing mutations, innocent variants and all in between. Graphical displays and utilities. Find ...

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