(Q35934030)

English

Ashkenazi Jewish genetic disorders

scientific article

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

1 reference

Europe PubMed Central

Ashkenazi Jewish genetic disorders (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

author name string

Joel Charrow

1

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

publication date

1 January 2004

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

Familial Cancer

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

3-4

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

201-206

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

https://scigraph.springernature.com/pub.10.1007/s10689-004-9545-z

0 references

Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease: consensus recommendations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Dor Yeshorim story: community-based carrier screening for Tay-Sachs disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

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Protection afforded by sickle-cell trait against subtertian malareal infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

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Miglustat. Oxford GlycoSciences/Actelion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of primary dystonias and related disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delayed symptom onset and increased life expectancy in Sandhoff disease mice treated with N-butyldeoxynojirimycin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher disease. Enzymology, genetics, and treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme Polymorphisms in Man

1 reference

https://pubmed.ncbi.nlm.nih.gov/15516842

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10689-004-9545-Z

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 August 2017

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