(Q35643889)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

W J Kimberling

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

M D Weston

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

C Möller

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

A van Aarem

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

C W Cremers

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

J Sumegi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

P S Ing

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

C Connolly

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

A Martini

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

M Milani

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

language of work or name

English

0 references

publication date

1 January 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

26 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

56

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

page(s)

216-223

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

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

26 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Transforming growth factor-beta in neural embryogenesis and neoplasia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Usher syndrome: definition and estimate of prevalence from two high-risk populations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Usher's syndrome--deafness and progressive blindness. Clinical cases, prevention, theory and literature survey

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Usher syndrome: an otoneurologic study.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Progressive hearing loss in Usher's syndrome.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Localization of Usher syndrome type II to chromosome 1q.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

The CEPH consortium linkage map of human chromosome 1

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Cloning of a human homeobox gene that resembles a diverged Drosophila homeobox gene and is expressed in activated lymphocytes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Dinucleotide repeat polymorphism at the human poly (ADP-ribose) polymerase gene (PPOL)

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

A second-generation linkage map of the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Dinucleotide repeat polymorphism for D1S70 (CRI-L461) on chromosome 1q41.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Dinucleotide repeat polymorphism in the TGFB2 gene

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801344

Transforming growth factor-beta control of cell-substratum adhesion during avian neural crest cell emigration in vitro

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7825581

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Dystrophia retinae pigmentosa--dysacusis syndrome (DRD): a study of the Usher- or Hallgren syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7825581

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A simple reproducible method for prometaphase chromosome analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7825581

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7825581%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

PubMed publication ID

7825581

1 reference