(Q30495384)

6 October 2017

Genetic heterogeneity of Usher syndrome type II (English)

1 reference

6 October 2017

1 reference

1 reference

S Pieke Dahl

1

1 reference

6 October 2017

W J Kimberling

2

1 reference

6 October 2017

M B Gorin

3

1 reference

6 October 2017

M D Weston

4

1 reference

6 October 2017

J M Furman

5

1 reference

6 October 2017

A Pikus

6

1 reference

6 October 2017

C Möller

7

1 reference

6 October 2017

language of work or name

English

0 references

publication date

1 October 1993

1 reference

Journal of Medical Genetics

6 October 2017

1 reference

6 October 2017

30

1 reference

6 October 2017

10

1 reference

6 October 2017

843-848

1 reference

Retinitis pigmentosa combined with congenital deafness; with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: A clinical and genetico-statistical study

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Usher's syndrome type III: ENG findings in four affected and six unaffected siblings

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Usher syndrome: an otoneurologic study.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Usher syndrome: clinical findings and gene localization studies.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Localization of Usher syndrome type II to chromosome 1q.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

The CEPH consortium linkage map of human chromosome 1

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneity.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Localization of two genes for Usher syndrome type I to chromosome 11.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

A gene for Usher syndrome type I (USH1A) maps to chromosome 14q

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Usher's Syndrome Type III

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016567

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

20 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7901420

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.30.10.843

1 reference

6 October 2017

1 reference

6 October 2017

PubMed publication ID

7901420

1 reference