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. (Q52096452)

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scientific article published in January 1983

Language	Label	Description	Also known as
English	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.	scientific article published in January 1983

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

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. (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

1 reference

based on heuristic

inferred from title

author name string

P Steinbach

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

G Barbi

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

S Baur

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

W Vogel

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

publication date

1 January 1983

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

64

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

279-282

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of fra(X)(q28) is suppressed in man-mouse hybrid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative radiochemical enzyme assays in single cells: Purine phosphoribosyl transferase activities in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hurler's syndrome: a genetic study of clones in cell culture with particular reference to the Lyon hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

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/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonspecific X-linked mental retardation--a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activity of the fragile X in heterozygous carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A marker X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cocultivation studies with cells of patients bearing fragile X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6885072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00279411

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6885072

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