(Q41496851)

1 October 2017

Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1. (English)

1 reference

juvenile neuronal ceroid lipofuscinosis

1 October 2017

0 references

disequilibrium

1 reference

inferred from title

linkage disequilibrium

1 reference

8

J L Haines

1 reference

1 October 2017

7

J F Gusella

1 reference

1 October 2017

2

R M Boustany

1 reference

1 October 2017

Xandra O. Breakefield

6

object named as

X O Breakefield

1 reference

1 October 2017

T J Lerner

1

1 reference

1 October 2017

K MacCormack

3

1 reference

1 October 2017

J Gleitsman

4

1 reference

1 October 2017

K Schlumpf

5

1 reference

1 October 2017

language of work or name

English

0 references

publication date

1 January 1994

1 reference

American Journal of Human Genetics

1 October 2017

1 reference

1 October 2017

54

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1 October 2017

88-94

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1 October 2017

1

1 reference

Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

An index marker map of chromosome 9 provides strong evidence for positive interference

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Strategies for multilocus linkage analysis in humans

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Reconsideration of the classification of the neuronal ceroid-lipofuscinoses.

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Clinical classification of neuronal ceroid-lipofuscinosis subtypes.

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Clinico-pathological variability in the childhood neuronal ceroid-lipofuscinoses and new observations on glycoprotein abnormalities.

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Batten disease: past, present, and future.

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Identification of the cystic fibrosis gene: genetic analysis

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16.

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Dinucleotide repeat polymorphism (D16S285) on human chromosome 16

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Molecular analysis of human chromosome 16 cosmid clones containing NotI sites

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

High-resolution cytogenetic-based physical map of human chromosome 16.

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

The Huntington's disease candidate region exhibits many different haplotypes

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918064

Batten disease (Spielmeyer-Sjøgren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16

19 August 2018

1 reference

12 December 2020

Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1

1 reference

12 December 2020

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

1 reference

12 December 2020

Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci

1 reference

12 December 2020

Identifiers

1 reference

1 October 2017

1 reference