Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. (Q35200306)

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8 October 2019

title

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

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8 October 2019

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Mulligan LM

1

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8 October 2019

Phillips MA

2

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8 October 2019

Forster-Gibson CJ

3

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8 October 2019

Beckett J

4

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8 October 2019

Partington MW

5

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8 October 2019

Simpson NE

6

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8 October 2019

Holden JJ

7

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8 October 2019

White BN

8

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8 October 2019

language of work or name

English

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publication date

1 May 1985

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American Journal of Human Genetics

8 October 2019

published in

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8 October 2019

volume

37

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8 October 2019

issue

3

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8 October 2019

page(s)

463-472

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Gene deletions in patients with haemophilia B and anti-factor IX antibodies

8 October 2019

cites work

1 reference

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The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males

28 July 2018

1 reference

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The fragile X syndrome II: preliminary data on growth and development in males

28 July 2018

1 reference

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The fragile X: a scanning electron microscope study

28 July 2018

1 reference

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Brief report: linkage between G6PD and fragile-X syndrome

28 July 2018

1 reference

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The fragile X syndrome: the patients and their chromosomes

28 July 2018

1 reference

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The fragile X chromosome.

28 July 2018

1 reference

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

28 July 2018

1 reference

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A polymorphic DNA marker genetically linked to Huntington's disease

28 July 2018

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

28 July 2018

1 reference

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A clinically useful DNA probe closely linked to haemophilia A

28 July 2018

1 reference

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Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684592

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684592

Detection of specific sequences among DNA fragments separated by gel electrophoresis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684592

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684592

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684592

Assay for Epstein-Barr virus based on stimulation of DNA synthesis in mixed leukocytes from human umbilical cord blood

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684592

Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684592

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=1684592

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=1684592

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

26 September 2018

1 reference

12 December 2020

Application of DNA analysis to mapping the human genome

1 reference

12 December 2020

Genetic mapping: X chromosome

1 reference

12 December 2020

Carrier detection by direct gene analysis in a family with haemophilia B (factor IX deficiency)

1 reference

12 December 2020

The fragile-X syndrome, IV. Progress towards the identification of linked restriction fragment length variants (RFLVs)

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2988332%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

PubMed publication ID

2988332

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