(Q35203588)

7 August 2017

The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin (English)

1 reference

7 August 2017

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1

Petersen GM

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7 August 2017

3

Cantor RM

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7 August 2017

Rotter JI

2

1 reference

7 August 2017

Field LL

4

1 reference

7 August 2017

Greenwald S

5

1 reference

7 August 2017

Lim JS

6

1 reference

7 August 2017

Roy C

7

1 reference

7 August 2017

Schoenfeld V

8

1 reference

7 August 2017

Lowden JA

9

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7 August 2017

Kaback MM

10

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7 August 2017

language of work or name

English

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publication date

1 November 1983

1 reference

American Journal of Human Genetics

7 August 2017

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7 August 2017

35

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7 August 2017

1258-1269

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7 August 2017

6

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Heterozygote advantage in Tay-Sachs carriers?

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Estimation of the frequency of hexosaminidase a variant alleles in the American Jewish population

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Population dynamics of Tay-Sachs disease. I. Reproductive fitness and selection

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Founder effect in Tay-Sachs disease unlikely

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Controversy in human genetics: founder effect in Tay-Sachs disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Automated assay of hexosaminidases in serum.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Approaches to the control and prevention of Tay-Sachs disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Elevated frequency of Tay-Sachs disease among Ashkenazic Jews unlikely by genetic drift alone

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

Tay-Sachs disease: a genetic-historical view of selective advantage

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685967

On the maintenance of polymorphisms having an inviable homozygote

13 July 2018

1 reference

12 December 2020

Tay-Sachs disease: genetic drift among the Ashkenazim Jews

1 reference

12 December 2020

Infantile amaurotic family idiocy; a genetic approach

1 reference

12 December 2020

A genetic profile of infantile amaurotic family idiocy; statistical evaluation of one hundred thirty-one patients

1 reference

12 December 2020

Identifiers

PMCID

1685967

1 reference

7 August 2017

1 reference