(Q34626986)

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

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scholarly article

1 reference

Europe PubMed Central

3 August 2017

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

1 reference

Europe PubMed Central

3 August 2017

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George P Patrinos

3

object named as

George P Patrinos

1 reference

Europe PubMed Central

3 August 2017

author name string

Joël Zlotogora

1

1 reference

Europe PubMed Central

3 August 2017

Sjozef van Baal

2

1 reference

Europe PubMed Central

3 August 2017

publication date

1 October 2007

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Europe PubMed Central

3 August 2017

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Europe PubMed Central

3 August 2017

28

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Europe PubMed Central

3 August 2017

944-949

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Europe PubMed Central

3 August 2017

10

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Europe PubMed Central

3 August 2017

Consanguineous matings in an Israeli-Arab community

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

21 January 2018

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.20551

7 January 2021

based on heuristic

inferred from DOI database lookup

Consanguinity, intracommunity and intercommunity marriages in a population sample of Israeli Jews

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

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HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

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Changing marriage systems in the Jewish communities of Israel

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

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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.20551

7 January 2021

based on heuristic

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Trends in the frequencies of consanguineous marriages in the Israeli Arab community

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

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The cypriot and Iranian National Mutation Frequency Databases.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

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GeneTests-GeneClinics: genetic testing information for a growing audience

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

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Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

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DNA, diseases and databases: disastrously deficient

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

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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.20551

7 January 2021

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National and ethnic mutation databases: recording populations' genography

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

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PAHdb 2003: what a locus-specific knowledgebase can do.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

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Database for the mutations of the Finnish disease heritage

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

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CTGA: the database for genetic disorders in Arab populations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

inferred from DOI database lookup

Singapore Human Mutation/Polymorphism Database: a country-specific database for mutations and polymorphisms in inherited disorders and candidate gene association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

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Arab genetic disease database (AGDDB): a population-specific clinical and mutation database

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive diseases among Palestinian Arabs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular basis of mendelian disorders among Jews

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20551

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20551

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

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