Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304). (Q35197242)

7 August 2017

title

Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304). (English)

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7 August 2017

Dahl N

1

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7 August 2017

Goonewardena P

2

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7 August 2017

Malmgren H

3

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7 August 2017

Gustavson KH

4

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7 August 2017

Holmgren G

5

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7 August 2017

Seemanova E

6

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7 August 2017

Annerén G

7

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7 August 2017

Flood A

8

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7 August 2017

Pettersson U

9

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7 August 2017

language of work or name

English

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publication date

1 August 1989

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

45

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7 August 2017

issue

2

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7 August 2017

page(s)

304-309

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Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

7 August 2017

cites work

1 reference

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

13 July 2018

1 reference

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Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.

13 July 2018

1 reference

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

13 July 2018

1 reference

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

13 July 2018

1 reference

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Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683358

Fragile X syndrome: growth, development, and intellectual function

13 July 2018

1 reference

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Multilocus analysis of the fragile X syndrome.

13 July 2018

1 reference

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Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere

13 July 2018

1 reference

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

13 July 2018

1 reference

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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).

13 July 2018

1 reference

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Linkage studies in a large fragile X family

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683358

Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683358

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683358

Molecular genetics of hemophilia A in man (factor VIII deficiency).

13 July 2018

1 reference

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The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683358

RFLP for linkage analysis of fragile X syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683358

Detection of specific sequences among DNA fragments separated by gel electrophoresis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683358

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

13 July 2018

1 reference

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

26 September 2018

1 reference

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Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

26 September 2018

1 reference

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Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis

26 September 2018

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12 December 2020

Preventive screening for the fragile X syndrome

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12 December 2020

Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome

1 reference

12 December 2020

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

12 December 2020

Identifiers

PMC publication ID

1683358

1 reference

7 August 2017

1 reference