DNA restriction fragment length polymorphisms and heterozygosity in the human genome (Q40140388)

17 September 2017

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title

DNA restriction fragment length polymorphisms and heterozygosity in the human genome (English)

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17 September 2017

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1

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17 September 2017

J Schmidtke

2

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17 September 2017

language of work or name

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1 January 1984

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17 September 2017

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17 September 2017

volume

66

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17 September 2017

issue

1

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17 September 2017

page(s)

1-16

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Globin mRNA Sequences: Analysis of Base Pairing and Evolutionary Implications

17 September 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FBF00275182

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

21 January 2018

1 reference

12 December 2020

Translocation and rearrangements of the c-myc oncogene locus in human undifferentiated B-cell lymphomas

1 reference

12 December 2020

Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism

1 reference

12 December 2020

Eukaryotic DNA methylation

1 reference

12 December 2020

Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.

1 reference

12 December 2020

A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

1 reference

12 December 2020

Human metallothionein genes--primary structure of the metallothionein-II gene and a related processed gene

1 reference

12 December 2020

Inherited deletion of immunoglobulin heavy chain constant region genes in normal human individuals

1 reference

12 December 2020

The human gene map, 20 October 1982

1 reference

12 December 2020

DNA methylation and the frequency of CpG in animal DNA.

1 reference

12 December 2020

Higher frequencies of transitions among point mutations

1 reference

12 December 2020

Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

12 December 2020

Report of the committee on human gene mapping by recombinant DNA techniques. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping.

1 reference

12 December 2020

The prolactin gene is located on chromosome 6 in humans

1 reference

12 December 2020

Confirmation of Y/autosome translocations using recombinant DNA

1 reference

12 December 2020

An inherited polymorphism in the human apolipoprotein A-I gene locus related to the development of atherosclerosis

1 reference

12 December 2020

A highly polymorphic locus in human DNA

1 reference

12 December 2020

Sequence of human haptoglobin cDNA: evidence that the α and β subunits are coded by the same mRNA

1 reference

12 December 2020

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

1 reference

12 December 2020

Polymorphism of the Hinf I restriction site located 1 Kb 5' to the human beta-globin gene

1 reference

12 December 2020

A new DNA polymorphism in the beta-globin gene cluster can be used for antenatal diagnosis of beta-thalassaemia

1 reference

12 December 2020

Polymorphism in the 5′-Flanking Region of the Human Insulin Gene and Its Possible Relation to Type 2 Diabetes

1 reference

12 December 2020

Assignment of the structural gene coding for albumin to human chromosome 4

1 reference

12 December 2020

A Hind III restriction site polymorphism in the human collagen ?1(I)-like gene on chromosome No. 7

1 reference

12 December 2020

Highly variable regions of DNA flank the human alpha globin genes

1 reference

12 December 2020

Studies on mutant human insulin genes: identification and sequence analysis of a gene encoding [SerB24]insulin

1 reference

12 December 2020

Sequence of the human insulin gene

1 reference

12 December 2020

Structure of the human immune interferon gene

1 reference

12 December 2020

Analysis of the regions flanking the human insulin gene and sequence of an Alu family member

1 reference

12 December 2020

Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase

1 reference

12 December 2020

Polymorphism and complexity of the human DC and murine I-A alpha chain genes

1 reference

12 December 2020

Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia

1 reference

12 December 2020

Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome

1 reference

12 December 2020

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

12 December 2020

Molecular analysis of argininosuccinate synthetase deficiency in human fibroblasts

1 reference

12 December 2020

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12 December 2020

Polymorphic restriction endonuclease fragment segregates and correlates with the gene for HLA-B8

1 reference

12 December 2020

Two types of triplicateda-globin loci in humans

1 reference

12 December 2020

Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments

1 reference

12 December 2020

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

1 reference

12 December 2020

Two nonallelic tRNAiMet genes are located in the p23 leads to q12 region of human chromosome 6

1 reference

12 December 2020

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

12 December 2020

Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion

1 reference

12 December 2020

The thalassemias: molecular mechanisms of human genetic disease.

1 reference

12 December 2020

Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

1 reference

12 December 2020

HLA-D region β-chain DNA endonuclease fragments differ between HLA-DR identical healthy and insulin-dependent diabetic individuals

1 reference

12 December 2020

Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides

1 reference

12 December 2020

Gamma thalassemia resulting from the deletion of a gamma-globin gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Amino acid change associated with the major polymorphic Hinc II site of Oriental and Caucasian mitochondrial DNAs

1 reference

12 December 2020

Polymorphism in the 5′ Flanking Region of the Human Insulin Gene: A Genetic Marker for Non-Insulin-Dependent Diabetes

1 reference

12 December 2020

Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis

1 reference

12 December 2020

Detection of HLA-D/DR-related DNA polymorphism in HLA-D homozygous typing cells

1 reference

12 December 2020

HeLa cell identification by analysis of ribosomal DNA segment patterns generated by endonuclease restriction

1 reference

12 December 2020

Isolation and characterization of human actin genes

1 reference

12 December 2020

T24 human bladder carcinoma oncogene is an activated form of the normal human homologue of BALB- and Harvey-MSV transforming genes

1 reference

12 December 2020

The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences

1 reference

12 December 2020

The scattered distribution of actin genes in the mouse and human genomes

1 reference

12 December 2020

Recombination within and between the human insulin and beta-globin gene loci

1 reference

12 December 2020

The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA

1 reference

12 December 2020

Molecular basis of base substitution hotspots in Escherichia coli

1 reference

12 December 2020

Clustered arrangement of immunoglobulin λ constant region genes in man

1 reference

12 December 2020

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

1 reference

12 December 2020

Optimal use of restriction enzymes in the analysis of human DNA polymorphism

1 reference

12 December 2020

Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

12 December 2020

How many polymorphic genes will it take to span the human genome?

1 reference

12 December 2020

Molecular Heterogeneity of Inherited Antithrombin III Deficiency

1 reference

12 December 2020

Allelic polymorphism and complexity of the genes for HLA-DR β-chains—direct analysis by DNA–DNA hybridization

1 reference

12 December 2020

Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variant

1 reference

12 December 2020

Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14.

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple arrangements of the human embryonic zeta globin genes

1 reference

12 December 2020

Application of DNA analysis to mapping the human genome

1 reference

12 December 2020

cDNA clones coding for the heavy chain of human HLA-DR antigen

1 reference

12 December 2020

A single gonadotropin alpha-subunit gene in normal tissue and tumor-derived cell lines

1 reference

12 December 2020

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

Characterization of a new aberration of the human Y chromosome by banding methods and DNA restriction endonuclease analysis

1 reference

12 December 2020

DNA methylation in the human γδβ-globin locus in erythroid and nonerythroid tissues

1 reference

12 December 2020

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

1 reference

12 December 2020

Human c-Ki-ras2 proto-oncogene on chromosome 12

1 reference

12 December 2020

Kpn I family of long interspersed repeated DNA sequences in primates: polymorphism of family members and evidence for transcription

1 reference

12 December 2020

Hypoxanthine-guanine phosphoribosyltransferase deficiency. The molecular basis of the clinical syndromes

1 reference

12 December 2020

Linkage of human apolipoproteins A-I and C-III genes

1 reference

12 December 2020

A new polymorphism in the human beta-globin gene useful in antenatal diagnosis

1 reference

12 December 2020

Extrachromosomal circular copies of an ‘inter-Alu’ unstable sequence in human DNA are amplified during in vitro and in vivo ageing

1 reference

12 December 2020

Cloning of human immunoglobulin epsilon chain genes: evidence for multiple C epsilon genes

1 reference

12 December 2020

A DNA insertion in the apolipoprotein A-I gene of patients with premature atherosclerosis

1 reference

12 December 2020

Human class II major histocompatibility antigen β-chains are derived from at least three loci

1 reference

12 December 2020

Variable amplification of immunoglobulin λ light-chain genes in human populations

1 reference

12 December 2020

Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA

1 reference

12 December 2020

Use of restriction endonucleases for mapping the allele for beta s-globin

1 reference

12 December 2020

Restriction endonuclease mapping of the human γ globin gene loci

1 reference

12 December 2020

Genome instability in a region of human DNA enriched in Alu repeat sequences

1 reference

12 December 2020

Direct identification of sickle cell anemia by blot hybridization

1 reference

12 December 2020

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

1 reference

12 December 2020

Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemia

1 reference

12 December 2020

Polymorphic human somatostatin gene is located on chromosome 3

1 reference

12 December 2020

Isolation and characterization of human myosin heavy chain genes

1 reference

12 December 2020

Rapid evolution of animal mitochondrial DNA

1 reference

12 December 2020

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation of a cDNA clone for human antithrombin III

1 reference

12 December 2020

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

12 December 2020

Average heterozygosity per locus in man: an estimate based on the incidence of enzyme polymorphisms

1 reference

12 December 2020

The mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease

1 reference

12 December 2020

Mapping the human genome, cloned genes, DNA polymorphisms, and inherited disease

1 reference

12 December 2020

Methylation and a Polymorphic Restriction Site Adjacent to Human β-Interferon Gene

1 reference

12 December 2020

Mechanism of activation of a human oncogene

1 reference

12 December 2020

Structure and multiplicity of genes for the human immunoglobulin heavy chain variable region

1 reference

12 December 2020

Processed genes: a dispersed human immunoglobulin gene bearing evidence of RNA-type processing

1 reference

12 December 2020

Analysis of the 3' end of the human pro-alpha 2(I) collagen gene. Utilization of multiple polyadenylation sites in cultured fibroblasts

1 reference

12 December 2020

Isolation of a cDNA clone for the human HLA-DR antigen alpha chain by using a synthetic oligonucleotide as a hybridization probe

1 reference

12 December 2020

α1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene

1 reference

12 December 2020

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

1 reference

12 December 2020

Isolation and preliminary characterization of a human transforming gene from T24 bladder carcinoma cells

1 reference

12 December 2020

Assigning the polymorphic human insulin gene to the short arm of chromosome 11 by chromosome sorting

1 reference

12 December 2020

Structure and variation of human ribosomal DNA: the external transcribed spacer and adjacent regions

1 reference

12 December 2020

Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta.

1 reference

12 December 2020

Mapping of the genes encoding the HLA-DR alpha chain and the HLA-related antigens to a chromosome 6 deletion by using genomic blotting

1 reference

12 December 2020

Isolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinase

1 reference

12 December 2020

Model for antenatal diagnosis of β-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms

1 reference

12 December 2020

Applications of polymorphisms in anthropogenetic studies.

1 reference

12 December 2020

Human nucleolus organizers on nonhomologous chromosomes can share the same ribosomal gene variants

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation of human C-reactive protein complementary DNA and localization of the gene to chromosome 1.

1 reference

12 December 2020

DNA POLYMORPHISM ADJACENT TO HUMAN APOPROTEIN A-1 GENE: RELATION TO HYPERTRIGLYCERIDAEMIA

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12 December 2020

Isolation of cDNA clones encoding HLA-DR alpha chains

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular basis for familial isolated growth hormone deficiency

1 reference

12 December 2020

Variation in the sequence and modification state of the human insulin gene flanking regions

1 reference

12 December 2020

Genetic analysis of familial isolated growth hormone deficiency type I

1 reference

12 December 2020

Polymorphism in the 5'-flanking region of the human insulin gene and the incidence of diabetes.

1 reference

12 December 2020

Non-randomness of base replacement in point mutation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00275182

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Dimensions Publication ID

17 September 2017

1043397192

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