(Q70187271)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3038730%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

title

Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3038730%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1 reference

J A Buchanan

1

1 reference

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9 October 2019

K E Buckton

2

1 reference

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9 October 2019

C M Gosden

3

1 reference

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9 October 2019

M S Newton

4

1 reference

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9 October 2019

J F Clayton

5

1 reference

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9 October 2019

S Christie

6

1 reference

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9 October 2019

N Hastie

7

1 reference

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9 October 2019

publication date

1 June 1987

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9 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3038730%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

volume

76

1 reference

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9 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3038730%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

page(s)

165-172

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https://scigraph.springernature.com/pub.10.1007/bf00284915

9 October 2019

exact match

0 references

cites work

Gene mapping and physical arrangements of human chromatin in transformed, hybrid cells: fluorescent and autoradiographic in situ hybridization compared.

1 reference

12 December 2020

New technique for distinguishing between human chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

1 reference

12 December 2020

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

12 December 2020

Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes.

1 reference

12 December 2020

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

1 reference

12 December 2020

Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling.

1 reference

12 December 2020

The genetic linkage map of the human X chromosome

1 reference

12 December 2020

Transmission of fragile (X) (q27) site from a male

1 reference

12 December 2020

Population incidence and segregation ratios in the Martin-Bell syndrome.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

12 December 2020

Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males

1 reference

12 December 2020

Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

1 reference

12 December 2020

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

1 reference

12 December 2020

A multipoint linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes

1 reference

12 December 2020

The female and the fragile X. A study of 144 obligate female carriers.

1 reference

12 December 2020

The use of cloned Y chromosome-specific DNA probes for fetal sex determination in first trimester prenatal diagnosis

1 reference

12 December 2020

Transmission of fragile (X)(q27) from normal male(s)

1 reference

12 December 2020

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

1 reference

12 December 2020

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

1 reference

12 December 2020

Prevalence of the fragile X syndrome in an institution for the mentally handicapped.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00284915

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3038730%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1 reference