A YAC contig across the fragile X site defines the region of fragility (Q40504593)

21 September 2017

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

1 reference

21 September 2017

Hirst MC

1

1 reference

21 September 2017

Rack K

2

1 reference

21 September 2017

Nakahori Y

3

1 reference

21 September 2017

Roche A

4

1 reference

21 September 2017

Bell MV

5

1 reference

21 September 2017

Flynn G

6

1 reference

21 September 2017

Christadoulou Z

7

1 reference

21 September 2017

MacKinnon RN

8

1 reference

21 September 2017

Francis M

9

1 reference

21 September 2017

Littler AJ

10

1 reference

21 September 2017

1 June 1991

1 reference

21 September 2017

Nucleic Acids Research

1 reference

21 September 2017

19

1 reference

21 September 2017

12

1 reference

21 September 2017

3283-3288

1 reference

21 September 2017

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=328323

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

The frequency of the fragile X chromosome among schoolchildren in Coventry

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Yeast artificial chromosomes containing human Xq24-Xq28 DNA: library construction and representation of probe sequences

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

A 3.5 genome equivalent multi access YAC library: construction, characterisation, screening and storage

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Yeast artificial chromosome cloning of a two-megabase-size contig within chromosomal band 18q21 establishes physical linkage between BCL2 and plasminogen activator inhibitor type-2.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

In situ hybridization to cytogenetic bands of yeast artificial chromosomes covering 50% of human Xq24-Xq28 DNA

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

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

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

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

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

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

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

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

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328323

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

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2062644

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2062644

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/19.12.3283

1 reference

21 September 2017

1 reference

21 September 2017

PubMed publication ID

2062644

1 reference