(Q35197670)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

title

Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

main subject

amelogenesis imperfecta

1 reference

Lagerström M

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Dahl N

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Iselius L

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Bäckman B

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Pettersson U

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

language of work or name

English

0 references

publication date

1 January 1990

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

21 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

volume

46

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

page(s)

120-125

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

A strategy to reveal high-frequency RFLPs along the human X chromosome

21 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Construction and identification of mouse amelogenin cDNA clones

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Demonstration of the lyon hypothesis in X-linked dominant hypoplastic amelogenesis imperfecta

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Inherited defects in tooth structure

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

The genetic linkage map of the human X chromosome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Human X chromosome markers and Duchenne muscular dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Amelogenesis imperfecta: a genetic study

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Human and mouse amelogenin gene loci are on the sex chromosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Detection of specific sequences among DNA fragments separated by gel electrophoresis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Easy calculations of lod scores and genetic risks on small computers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683539

Properties of dissociatively extracted fetal tooth matrix proteins. I. Principal molecular species in developing bovine enamel

26 September 2018

1 reference

12 December 2020

Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution

1 reference

12 December 2020

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X and Y chromosomes

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1967204%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

PubMed publication ID

1967204

1 reference