(Q24540209)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3. (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

0 references

0 references

1 reference

2

1 reference

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12 November 2019

Sylvie Gerber

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Isabelle Perrault

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Asma Smahi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

A Cabot

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

D Ducroq

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

E Souied

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

J Kaplan

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

A Munnich

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

language of work or name

English

0 references

publication date

1 April 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

12 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

volume

64

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

issue

4

1 reference

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12 November 2019

page(s)

1141-1146

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene

12 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Ultrastructural study of extraocular muscle in congenital nystagmus

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Familial mitochondrial myopathy with cataract

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Hereditary nystagmus in early childhood

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Foveation dynamics in congenital nystagmus. I: Fixation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Is the geniculostriate system a prerequisite for nystagmus?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Significance of nystagmus in suspected blindness in infancy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Hereditary congenital nystagmus. An intrafamilial study.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

VEP projections in congenital nystagmus; VEP asymmetry in albinism: a comparison study

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

A STUDY OF CONGENITAL NYSTAGMUS.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

A Gene for Autosomal Dominant Congenital Nystagmus Localizes to 6p12

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

Congenital nystagmus: A clinical perspective in infancy

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377838

29 November 2018

1 reference

12 December 2020

Prevalence and inheritance of congenital nystagmus in a Swedish population

1 reference

12 December 2020

Hereditary congenital nystagmus and gaze-holding failure: the role of the neural integrator

1 reference

12 December 2020

Congenital nystagmus: fine structure of human extraocular muscles

1 reference

12 December 2020

Congenital nystagmus: fine structure of human extraocular muscles

1 reference

12 December 2020

Foveation dynamics in congenital nystagmus. II: Smooth pursuit

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F302324

7 January 2021

inferred from DOI database lookup

Foveation dynamics in congenital nystagmus. III: Vestibulo-ocular reflex

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F302324

7 January 2021

inferred from DOI database lookup

Heredity and rheumatic fever; some later information about data collected in 1950-51.

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F302324

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/302324

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090899%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

PubMed publication ID

10090899

2 references