(Q33645526)

28 July 2017

Locus-specific database domain and data content analysis: evolution and content maturation toward clinical use. (English)

1 reference

28 July 2017

0 references

Adam J Webb

2

0 references

Anthony J Brookes

series ordinal

4

object named as

Anthony J Brookes

1 reference

28 July 2017

5

George P Patrinos

1 reference

28 July 2017

Christina Mitropoulou

series ordinal

1

1 reference

PubMed ID

20672379

28 July 2017

Konstantinos Mitropoulos

series ordinal

3

1 reference

28 July 2017

1 October 2010

1 reference

28 July 2017

1 reference

28 July 2017

31

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28 July 2017

1109-1116

1 reference

28 July 2017

10

1 reference

ETHNOS : A versatile electronic tool for the development and curation of national genetic databases

28 July 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

McKusick's Online Mendelian Inheritance in Man (OMIM)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

UMD (Universal Mutation Database): 2005 update

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Nomenclature for the description of human sequence variations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-box" approach

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

A database of locus-specific databases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Planning the human variome project: the Spain report.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

The cypriot and Iranian National Mutation Frequency Databases.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

National and ethnic mutation databases: recording populations' genography

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

DNA, diseases and databases: disastrously deficient

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

A new scientific journal linked to a genetic database: towards a novel publication modality

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

MUTbase: maintenance and analysis of distributed mutation databases.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

VariVis: a visualisation toolkit for variation databases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Human Gene Mutation Database (HGMD): 2003 update.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21332

7 January 2021

Identifiers

DOI

10.1002/HUMU.21332

1 reference

28 July 2017

1 reference

PubMed ID

20672379