Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium (Q35203040)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

title

Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium (English)

1 reference

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14 October 2019

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linkage disequilibrium

1 reference

A Chakravarti

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

language of work or name

English

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publication date

1 July 1983

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

14 October 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

volume

35

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14 October 2019

issue

4

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14 October 2019

page(s)

592-610

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json

Utility and efficiency of linked marker genes for genetic counseling. II. Identification of linkage phase by offspring phenotypes

14 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

A common mutant EcoRI restriction endonuclease site in the 5' flanking portion of the human alpha-globin gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Molecular basis for familial isolated growth hormone 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=1685725

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Early recognition of heterozygotes for the gene for dystrophia myotonica

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Use of Genetic Linkage for the Detection of Female Carriers of Hemophilia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Prenatal prediction in myotonic dystrophy: Guidelines for genetic counseling

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Widening the scope of antenatal diagnosis.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Prenatal diagnosis by linkage: hemophilia A and polymorphic glucose-6-phosphate deydrogenase

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Heterogeneity of DNA fragments associated with the sickle-globin gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Prenatal Diagnosis of Classic Hemophilia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Proportion of informative families for genetic counseling with linked marker genes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

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=1685725

Antenatal diagnosis of sickle-cell anaemia by D.N.A. analysis of amniotic-fluid cells

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

The sporadic case of haemophilia A.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725

Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites

26 September 2018

1 reference

12 December 2020

The use of genetic linkage in counselling families with dystrophia myotonica

1 reference

12 December 2020

Non-random association between electromorphs and inversion chromosomes in finite populations

1 reference

12 December 2020

Genetic diagnosis of the fetus

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1 reference