(Q35590590)

9 August 2017

title

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

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9 August 2017

10

Lathrop GM

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9 August 2017

Oberlé I

1

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9 August 2017

Heilig R

2

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9 August 2017

Moisan JP

3

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9 August 2017

Kloepfer C

4

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9 August 2017

Mattéi GM

5

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9 August 2017

Mattéi JF

6

1 reference

9 August 2017

Boué J

7

1 reference

9 August 2017

Froster-Iskenius U

8

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9 August 2017

Jacobs PA

9

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9 August 2017

language of work or name

English

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publication date

1 February 1986

1 reference

Proceedings of the National Academy of Sciences of the United States of America

9 August 2017

published in

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9 August 2017

volume

83

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9 August 2017

issue

4

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9 August 2017

page(s)

1016-1020

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The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Marker (X)-Linked Mental Retardation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

A polymorphic DNA marker genetically linked to Huntington's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Exclusion of haemophilia B in male fetus by chorionic villus biopsy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

15 Detection of specific RNAs or specific fragments of DNA by fractionation in gels and transfer to diazobenzyloxymethyl paper

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

X-linked mental retardation: a study of 7 families

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Marker X syndrome in an oriental family with probable transmission by a normal male

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Strategies for multilocus linkage analysis in humans

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Easy calculations of lod scores and genetic risks on small computers

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

The fragile X syndrome. A study of 83 families

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=323001

Analysis of crossingover in man

26 September 2018

1 reference

12 December 2020

Genetic linkage heterogeneity in the fragile X syndrome

1 reference

12 December 2020

Feasibility of fragile X chromosome prenatal diagnosis demonstrated

1 reference

12 December 2020

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

1 reference

12 December 2020

Mental retardation linked to fragility of chromosome X: current knowledge

1 reference

12 December 2020

First trimester prenatal diagnosis of a male fetus with fragile X

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.83.4.1016

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9 August 2017

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9 August 2017

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