(Q34388974)

1 August 2017

title

Congenital motor nystagmus linked to Xq26-q27. (English)

1 reference

1 August 2017

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Kerrison JB

1

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1 August 2017

Vagefi MR

series ordinal

2

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1 August 2017

Barmada MM

series ordinal

3

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1 August 2017

Maumenee IH

series ordinal

4

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1 August 2017

language of work or name

English

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publication date

1 February 1999

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

64

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1 August 2017

issue

2

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1 August 2017

page(s)

600-607

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Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12.

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

A metric map of humans: 23,500 loci in 850 bands

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Ocular and vision defects in preschool children

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Congenital nystagmus cosegregating with a balanced 7;15 translocation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Faster sequential genetic linkage computations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

SOX3 is an X-linked gene related to SRY

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Strategies for multilocus linkage analysis in humans

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Easy calculations of lod scores and genetic risks on small computers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Nystagmus in a female carrier of ocular albinism.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Cloning of a brain protein identified by autoantibodies from a patient with paraneoplastic cerebellar degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Cerebellar degeneration-related antigen: a highly conserved neuroectodermal marker mapped to chromosomes X in human and mouse

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Paraneoplastic cerebellar degeneration. I. A clinical analysis of 55 anti-Yo antibody-positive patients

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

Avoiding recomputation in linkage analysis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

A Gene for Autosomal Dominant Congenital Nystagmus Localizes to 6p12

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377771

A RARE TYPE OF HEREDITARY NYSTAGMUS WITH AUTOSOMAL-DOMINANT INHERITANCE AND SPECIAL PHENOMENON: VERTICAL NYSTAGMUS COMPONENT AND DISORDER OF THE VERTICAL AND HORIZONTAL OPTOKINETIC NYSTAGMUS

27 October 2018

1 reference

12 December 2020

Affected females in X-linked congenital stationary night blindness

1 reference

12 December 2020

Sex linked hereditary nystagmus

1 reference

12 December 2020

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

1 reference

12 December 2020

Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome

1 reference

12 December 2020

SOX3 gene maps near DXS984 in Xq27.1, within candidate regions for several X-linked disorders

1 reference

12 December 2020

Identifiers

DOI

10.1086/302244

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1 August 2017

1 reference

1 August 2017

1 reference