Molecular cloning and analysis of the fragile X region in man (Q33563651)

28 July 2017

Molecular cloning and analysis of the fragile X region in man (English)

1 reference

28 July 2017

3

1 reference

28 July 2017

A Dietrich

1

1 reference

28 July 2017

P Kioschis

2

1 reference

28 July 2017

B Gross

4

1 reference

28 July 2017

B Korn

5

1 reference

28 July 2017

S V Williams

6

1 reference

28 July 2017

D Sheer

7

1 reference

28 July 2017

D Heitz

8

1 reference

28 July 2017

I Oberle

9

1 reference

28 July 2017

D Toniolo

10

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 May 1991

1 reference

28 July 2017

Nucleic Acids Research

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28 July 2017

19

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28 July 2017

10

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28 July 2017

2567-2572

1 reference

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Isolation and characterization of a major tandem repeat family from the human X chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Alu sequences transcription in X. laevis oocytes: nuclear-cytoplasmic partitioning and evidence for 3' end processing reactions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Proposed mechanism of inheritance and expression of the human 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=328171

The fragile X site in somatic cell hybrids: an approach for molecular cloning of fragile sites.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Fragile X syndrome: a unique mutation in man.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

A new DNA marker tightly linked to the fragile X locus (FRAXA).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Population genetic consequences of the fragile-X syndrome, based on the X-inactivation imprinting model.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Cloning of the T gene required in mesoderm formation in the mouse

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Physical mapping across the fragile X: hypermethylation and clinical expression of the 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=328171

Two progenitor cells for human oogonia inferred from pedigree data and the X-inactivation imprinting model of the 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=328171

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

The polymorphic human DNA sequence D8S8 assigned to 8q13-21.1, close to the carbonic anhydrase gene cluster, by isotopic and nonisotopic in situ hybridization and by linkage analysis

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328171

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

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2041732

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2041732

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A long-range restriction map encompassing the cystic fibrosis locus and its closely linked genetic markers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2041732

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/19.10.2567

1 reference

28 July 2017

1 reference

28 July 2017

1 reference