(Q35196686)

7 August 2017

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers (English)

1 reference

7 August 2017

1 reference

1 reference

Richards RI

1

1 reference

7 August 2017

Shen Y

2

1 reference

7 August 2017

Holman K

3

1 reference

7 August 2017

Kozman H

4

1 reference

7 August 2017

Hyland VJ

5

1 reference

7 August 2017

Mulley JC

6

1 reference

7 August 2017

Sutherland GR

7

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 June 1991

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

48

1 reference

7 August 2017

1051-1057

1 reference

7 August 2017

6

1 reference

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

The X chromosome shows less genetic variation at restriction sites than the autosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Diagnostic molecular genetics of the fragile X.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683096

Genetic mapping of new RFLPs at Xq27–q28

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2035525

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2035525

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1683096

1 reference

7 August 2017

1 reference