(Q35889527)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

congenital muscular dystrophy

29 October 2019

main subject

congenital disorder

0 references

1 reference

inferred from title

linkage disequilibrium

1 reference

Toda T

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Ikegawa S

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Okui K

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Kondo E

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Saito K

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Fukuyama Y

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Yoshioka M

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Kumagai T

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Suzumori K

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Kanazawa I

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

language of work or name

English

0 references

publication date

1 November 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

29 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

volume

55

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

page(s)

946-950

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

29 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=1918318

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Abnormal localization of laminin subunits in muscular dystrophies

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Strategies for multilocus linkage analysis in humans

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Identification of the cystic fibrosis gene: genetic analysis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Membrane organization of the dystrophin-glycoprotein complex

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

A dinucleotide repeat polymorphism at the D9S127 locus

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

A dinucleotide repeat polymorphism at the D9S109 locus

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

A second-generation linkage map of the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Construction of a GT polymorphism map of human 9q

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

The Huntington's disease candidate region exhibits many different haplotypes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32–34

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

Integrated human genome-wide maps constructed using the CEPH reference panel.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918318

INDIRECT CYSTIC FIBROSIS CARRIER DETECTION

24 September 2018

1 reference

12 December 2020

Linkage map of human chromosome 9 microsatellite polymorphisms

1 reference

12 December 2020

Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993

1 reference

12 December 2020

1 reference

12 December 2020

CEPH Consortium Map of Chromosome 9

1 reference

12 December 2020

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

1 reference

12 December 2020

A genetic study of the Fukuyama type congenital muscular dystrophy

1 reference

12 December 2020

Purification of DNA from formaldehyde fixed and paraffin embedded human tissue

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7977357%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

PubMed publication ID

7977357

1 reference