(Q33595415)

28 July 2017

Population studies of the fragile X: a molecular approach (English)

1 reference

28 July 2017

Jacobs PA

1

1 reference

28 July 2017

Bullman H

2

1 reference

28 July 2017

Macpherson J

3

1 reference

28 July 2017

Youings S

4

1 reference

28 July 2017

Rooney V

5

1 reference

28 July 2017

Watson A

6

1 reference

28 July 2017

Dennis NR

7

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 June 1993

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

30

1 reference

28 July 2017

6

1 reference

28 July 2017

454-459

1 reference

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Population screening for fragile X

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016415

Preventive screening for the fragile X syndrome

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8326487

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8326487

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Evidence of founder chromosomes in fragile X syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8326487

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.30.6.454

1 reference

28 July 2017

1 reference

28 July 2017

1 reference