(Q41208218)

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X chromosome imprinting in fragile X syndrome

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 September 2017

X chromosome imprinting in fragile X syndrome (English)

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Europe PubMed Central

PubMed publication ID

28 September 2017

fragile X syndrome

1 reference

based on heuristic

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author name string

W D Yu

1

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

S L Wenger

2

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

M W Steele

3

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

publication date

1 October 1990

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Europe PubMed Central

PubMed publication ID

28 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

85

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Europe PubMed Central

PubMed publication ID

28 September 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

590-594

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

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/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychiatric disability in female carriers of the fragile X chromosome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intracellular folate distribution in cultured fibroblasts from patients with the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparisons of in vivo BrdU labeling methods and spontaneous sister chromatid exchange frequencies in regenerating murine liver and bone marrow cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new R-banding technique in clinical cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pattern of chromosomal replication in synchronized lymphocytes. I. Evaluation and application of methotrexate block

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple method to demonstrate the fragile X chromosome in fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Folate metabolism in cells from fragile X syndrome patients and carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of recombination in the evolvement of the fragile X mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting male

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

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/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Folate metabolism and chromosomal stability in the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication kinetics of X chromosomes in fibroblasts and lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00193580

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

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