(Q35196551)

7 August 2017

Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genome (English)

1 reference

7 August 2017

1 reference

A J Pakstis

1

1 reference

7 August 2017

P Heutink

2

1 reference

7 August 2017

D L Pauls

3

1 reference

7 August 2017

R Kurlan

4

1 reference

7 August 2017

B J van de Wetering

5

1 reference

7 August 2017

J F Leckman

6

1 reference

7 August 2017

L A Sandkuyl

7

1 reference

7 August 2017

J R Kidd

8

1 reference

7 August 2017

G J Breedveld

9

1 reference

7 August 2017

C M Castiglione

10

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 February 1991

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

48

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7 August 2017

2

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7 August 2017

281-294

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Strategies for multilocus linkage analysis in humans

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

A primary genetic linkage map for human chromosome 12.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Severity of Tourette's syndrome in one large kindred. Implication for determination of disease prevalence rate

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

The inheritance of Gilles de la Tourette's syndrome and associated behaviors. Evidence for autosomal dominant transmission

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

The nucleotide sequence of chicken smooth muscle myosin light chain two

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

A mapped set of genetic markers for human chromosome 9.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

A mapped set of DNA markers for human chromosome 15.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Family data support a dominant major gene for Tourette syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Report of the nomenclature committee and the 1989 catalog of mapped 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=1683024

Tourette's syndrome: current concepts

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Linkage analyses of multiple endocrine neoplasia, type 2A (MEN-2A) with 20 DNA polymorphisms: 5% of the genome excluded

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683024

Gilles de la Tourette Syndrome Is Not Linked to D2-Dopamine Receptor

26 September 2018

1 reference

12 December 2020

Twelve loci form a continuous linkage map for human chromosome 18

1 reference

12 December 2020

Familial pattern of Gilles de la Tourette syndrome

1 reference

12 December 2020

Familial pattern and transmission of Gilles de la Tourette syndrome and multiple tics

1 reference

12 December 2020

The risk of Tourette's syndrome and chronic multiple tics among relatives of Tourette's syndrome patients obtained by direct interview

1 reference

12 December 2020

Familial Tourette's syndrome: report of a large pedigree and potential for linkage analysis

1 reference

12 December 2020

Twenty-five loci form a continuous linkage map of markers for human chromosome 7

1 reference

12 December 2020

Segregation and linkage analyses of Tourette's syndrome and related disorders

1 reference

12 December 2020

Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome.

1 reference

12 December 2020

Identifiers

PMCID

1683024

1 reference

7 August 2017

1 reference