(Q42951227)

11 November 2017

Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1. (English)

1 reference

11 November 2017

1 reference

G Haberhausen

1

1 reference

11 November 2017

I Schmitt

2

1 reference

11 November 2017

A Köhler

3

1 reference

11 November 2017

U Peters

4

1 reference

11 November 2017

S Rider

5

1 reference

11 November 2017

J Chelly

6

1 reference

11 November 2017

J D Terwilliger

7

1 reference

11 November 2017

A P Monaco

8

1 reference

11 November 2017

U Müller

9

1 reference

11 November 2017

language of work or name

English

0 references

publication date

1 September 1995

1 reference

American Journal of Human Genetics

11 November 2017

1 reference

11 November 2017

57

1 reference

11 November 2017

3

1 reference

11 November 2017

644-650

1 reference

Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans

11 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

The p250 subunit of native TATA box-binding factor TFIID is the cell-cycle regulatory protein CCG1.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Connexin mutations in X-linked Charcot-Marie-Tooth disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Familial half cryptic translocation t(9;17).

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Cloning and expression of human TAFII250: a TBP-associated factor implicated in cell-cycle regulation

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Nonuniform recombination within the human beta-globin gene cluster

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Molecular cloning of the cDNA of human X chromosomal gene (CCG1) which complements the temperature-sensitive G1 mutants, tsBN462 and ts13, of the BHK cell line

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

A procedure for in vitro amplification of DNA segments that lie outside the boundaries of known sequences

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Cloning and characterization of human and rat liver cDNAs coding for a gap junction protein

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Complex patterns of linkage disequilibrium in the Huntington disease region

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Delineation of the dystonia-parkinsonism syndrome locus in Xq13

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

The X-linked dystonia-parkinsonism syndrome (XDP): clinical and molecular genetic analysis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Isolation of DNTR polymorphisms from yeast artificial chromosomes encompassing X chromosomal loci PGK1 and DXS56

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Dinucleotide repeat polymorphism at the DXS559 locus

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801270

Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysis

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7668293

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The phenotype of the X-linked dystonia-parkinsonism syndrome. An assessment of 42 cases in the Philippines

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7668293

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7668293

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

11 November 2017

PubMed publication ID

7668293

1 reference