(Q46867079)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

A distinct autosomal recessive ataxia maps to chromosome 12 in an inbred family from Jordan (English)

1 reference

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14 January 2020

1

1 reference

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14 January 2020

Kwanghyuk Lee

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Kwanghyuk Lee

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

4

Suzanne M Leal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

author name string

Azhar Daoud

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Ammar A Sadoon

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Shan Chen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Ronald Spiegel

8

1 reference

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14 January 2020

publication date

10 January 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

published in

Brain and Development

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

volume

28

1 reference

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14 January 2020

issue

6

1 reference

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14 January 2020

page(s)

353-357

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

A combined linkage-physical map of the human genome

14 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Molecular background of progressive myoclonus epilepsy

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Allegro, a new computer program for multipoint linkage analysis

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Two genes are responsible for Griscelli syndrome at the same 15q21 locus.

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Faster sequential genetic linkage computations

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Progressive myoclonus epilepsies: specific causes and diagnosis

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Consanguineous marriage in Jordan

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6143173

Fast and sensitive silver staining of DNA in polyacrylamide gels

1 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16376507

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.BRAINDEV.2005.11.003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16376507%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference