(Q33674079)

English

Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

Connor JM

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Pirrit LA

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Yates JR

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Crossley JA

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Imrie SJ

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Colgan JM

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 January 1987

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

24

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

14-22

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

The fragile X: a scanning electron microscope study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Brief report: linkage between G6PD and fragile-X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

The fragile X syndrome: the patients and their chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Conference report: International Workshop on the fragile X and X-linked mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Marker (X)-Linked Mental Retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

The genetic linkage map of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Carrier testing strategy in haemophilia A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

30 October 2018

The fragile X syndrome. A study of 83 families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049851

30 October 2018

Chiasma derived genetic lengths and recombination fractions: chromosomes 2 and 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping: X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage heterogeneity in the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the gene for dyskeratosis congenita to Xq28

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879932

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.24.1.14

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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