(Q52090614)

English

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

scientific article published in January 1985

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome). (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

author name string

K E Davies

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

M G Mattei

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

J F Mattei

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

H Veenema

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

S McGlade

5

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

K Harper

6

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

N Tommerup

7

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

K B Nielsen

8

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

M Mikkelsen

9

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

P Beighton

10

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

publication date

1 January 1985

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

70

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

249-255

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

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/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of the gene for human anti-haemophilic factor IX.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinically useful DNA probe closely linked to haemophilia A

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationships of X-linked enzymes glucose-6-phosphate dehydrogenase and hypoxanthine guanine phosphoribosyltransferase: recombination in female offspring of compound heterozygotes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

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/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation with an X chromosome abnormality

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytological map of the human X chromosome--evidence for non-random recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

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/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Familial mental retardation and the fragile X syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of fragile X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Christmas disease, color-blindness and blood group Xga

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The application of DNA recombinant technology to the analysis of the human genome and genetic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X chromosome in a large Indian kindred.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of color blindness to hemophilias A and B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the human factor IX gene by molecular hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

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/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutional chromosomal breakage

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of sickle variant gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High resolution banding and the locus of the Xq fragile site

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for fra(X)(q) in a population of mentally retarded males

1 reference

https://pubmed.ncbi.nlm.nih.gov/2991115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00273451

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/2991115

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