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Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
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
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
main subject
disequilibrium
1 reference
based on heuristic
inferred from title
linkage disequilibrium
1 reference
based on heuristic
inferred from title
author name string
A Chakravarti
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
language of work or name
English
0 references
publication date
1 July 1983
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
volume
35
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
page(s)
592-610
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
cites work
Utility and efficiency of linked marker genes for genetic counseling. II. Identification of linkage phase by offspring phenotypes
1 reference
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PubMed Central
reference URL
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Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster
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28 July 2018
Nonrandom association of polymorphic restriction sites in the β-globin gene cluster
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725
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28 July 2018
A common mutant EcoRI restriction endonuclease site in the 5' flanking portion of the human alpha-globin gene
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Molecular basis for familial isolated growth hormone deficiency
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28 July 2018
Polymorphic DNA region adjacent to the 5' end of the human insulin gene
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28 July 2018
Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability
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28 July 2018
Early recognition of heterozygotes for the gene for dystrophia myotonica
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28 July 2018
Use of Genetic Linkage for the Detection of Female Carriers of Hemophilia
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28 July 2018
Prenatal prediction in myotonic dystrophy: Guidelines for genetic counseling
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28 July 2018
Widening the scope of antenatal diagnosis.
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28 July 2018
The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease
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28 July 2018
Prenatal diagnosis by linkage: hemophilia A and polymorphic glucose-6-phosphate deydrogenase
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28 July 2018
Heterogeneity of DNA fragments associated with the sickle-globin gene
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28 July 2018
Prenatal Diagnosis of Classic Hemophilia
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28 July 2018
Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725
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28 July 2018
Proportion of informative families for genetic counseling with linked marker genes
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725
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28 July 2018
Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation
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28 July 2018
Antenatal diagnosis of sickle-cell anaemia by D.N.A. analysis of amniotic-fluid cells
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28 July 2018
The sporadic case of haemophilia A.
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28 July 2018
The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725
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26 September 2018
Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685725
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26 September 2018
Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6576632
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The use of genetic linkage in counselling families with dystrophia myotonica
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6576632
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Non-random association between electromorphs and inversion chromosomes in finite populations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6576632
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genetic diagnosis of the fetus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6576632
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1685725
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
PubMed publication ID
6576632
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685725
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6576632%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
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