(Q35195069)

7 August 2017

title

Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis (English)

1 reference

familial Mediterranean fever

7 August 2017

main subject

1 reference

1 reference

Aksentijevich I

1

1 reference

7 August 2017

Pras E

2

1 reference

7 August 2017

Gruberg L

3

1 reference

7 August 2017

Shen Y

4

1 reference

7 August 2017

Holman K

5

1 reference

7 August 2017

Helling S

6

1 reference

7 August 2017

Prosen L

7

1 reference

7 August 2017

Sutherland GR

8

1 reference

7 August 2017

Richards RI

9

1 reference

7 August 2017

Dean M

10

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 September 1993

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

53

1 reference

7 August 2017

issue

3

1 reference

7 August 2017

page(s)

644-651

1 reference

Testing Hypotheses about Linkage Disequilibrium with Multiple Alleles

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Familial Mediterranean fever. A survey of 470 cases and review of the literature

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Identification of the cystic fibrosis gene: genetic analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Tay-Sachs disease in Moroccan Jews: deletion of a phenylalanine in the alpha-subunit of beta-hexosaminidase

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

High-resolution cytogenetic-based physical map of human chromosome 16.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682431

Linkage disequilibrium among multiple neutral alleles produced by mutation in finite 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=1682431

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8102507

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8102507

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8102507

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1682431

1 reference

7 August 2017

1 reference