A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. (Q33905215)

29 July 2017

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A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. (English)

1 reference

dyschromatosis symmetrica hereditaria

29 July 2017

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author name string

Qing-he Xing

1

1 reference

29 July 2017

Ming-tai Wang

2

1 reference

29 July 2017

Xiang-dong Chen

3

1 reference

29 July 2017

Guo-yin Feng

4

1 reference

29 July 2017

Hong-yun Ji

5

1 reference

29 July 2017

Jian-dong Yang

6

1 reference

29 July 2017

Jian-jun Gao

7

1 reference

29 July 2017

Wei Qin

8

1 reference

29 July 2017

Xue-qing Qian

9

1 reference

29 July 2017

Sheng-nan Wu

10

1 reference

29 July 2017

Lin He

11

1 reference

29 July 2017

language of work or name

English

0 references

publication date

12 June 2003

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

73

1 reference

29 July 2017

2

1 reference

29 July 2017

377-382

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Mutant laboratory mice with abnormalities in pigmentation: annotated tables

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Evolution of the regulators of G-protein signaling multigene family in mouse and human

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

A locus for brachydactyly type A-1 maps to chromosome 2q35-q36.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

RGS proteins: more than just GAPs for heterotrimeric G proteins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Familial reticulate acropigmentation of Dohi

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Homologous pigmentation mutations in human, mouse and other model organisms.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

A comprehensive genetic map of the human genome based on 5,264 microsatellites

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Easy calculations of lod scores and genetic risks on small computers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Multiple lentigines syndrome. Case report and review of the literature

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

A procedure for combining two-point lod scores into a summary multipoint map.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Dyschromatosis symmetrica hereditaria in an Indian family

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180374

Reticulate acropigmentation of Dohi: a case report of autosomal recessive inheritance

29 October 2018

1 reference

12 December 2020

Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum

1 reference

12 December 2020

The novel gene locus for agenesis of permanent teeth (He-Zhao deficiency) maps to chromosome 10q11.2.

1 reference

12 December 2020

The genetics of the hereditary xeroderma pigmentosum syndrome

1 reference

12 December 2020

Clinical and photobiological differences between dyschromatosis symmetrica hereditaria and xeroderma pigmentosum

1 reference

12 December 2020

Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report

1 reference

12 December 2020

Reticulate acropigmentation of Dohi

1 reference

12 December 2020

Neurofibromatosis and reticulate acropigmentation of Dohi: a case report

1 reference

12 December 2020

Identifiers

DOI

10.1086/377007

1 reference

29 July 2017

1 reference

29 July 2017

1 reference