(Q35776375)

10 August 2017

title

Molecular heterogeneity of the fragile X syndrome (English)

1 reference

10 August 2017

1 reference

1 reference

Y Nakahori

1

1 reference

10 August 2017

S J Knight

2

1 reference

10 August 2017

J Holland

3

1 reference

10 August 2017

C Schwartz

4

1 reference

10 August 2017

A Roche

5

1 reference

10 August 2017

J Tarleton

6

1 reference

10 August 2017

S Wong

7

1 reference

10 August 2017

T J Flint

8

1 reference

10 August 2017

U Froster-Iskenius

9

1 reference

10 August 2017

D Bentley

10

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 August 1991

1 reference

10 August 2017

published in

Nucleic Acids Research

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10 August 2017

volume

19

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10 August 2017

issue

16

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10 August 2017

page(s)

4355-4359

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

12 July 2018

A marker X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

The frequency of the fragile X chromosome among schoolchildren in Coventry

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

A YAC contig across the fragile X site defines the region of fragility

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

Linear order of new and established DNA markers around the fragile site at Xq27.3.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

The marker (X) syndrome: a cytogenetic and genetic analysis.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328620

Prevalence of the fragile X syndrome in four birth cohorts of children of school age

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1886762

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Unusual presentation of fragile X syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1886762

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/19.16.4355

1 reference

10 August 2017

1 reference

10 August 2017

1 reference