Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardation. (Q52049485)

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scientific article published in August 1991

Language	Label	Description	Also known as
English	Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardation.	scientific article published in August 1991

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardation. (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

author name string

D Wöhrle

1

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

P Steinbach

2

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

publication date

1 August 1991

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

87

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

4

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

421-424

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of nucleotides on expression of the folate sensitive fragile sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile-X mutation proposed to block complete reactivation in females of an inactive X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of thymidine, fluorodeoxyuridine, hydroxyurea, and methotrexate blocking at the G1/S phase transition of the cell cycle, studied by replication patterns

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features and reproductive patterns in fragile X female heterozygotes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Manifestation of the fragile site Xq27 in fibroblasts. III. A method to demonstrate R-type replication patterns and the fragile site

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologue

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A marker X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X syndrome. A study of 83 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1715307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00197160

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1715307

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