DNA typing in hereditary disease (Q68322151)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

review article

1 reference

title

DNA typing in hereditary disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

S. Wood

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1682336

28 October 2022

S. Langlois

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1682336

28 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1682336

28 October 2022

publication date

1 September 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

13 September 1991

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1682336

full work available at URL

28 October 2022

https://api.elsevier.com/content/article/PII:0378434791802414?httpAccept=text/xml

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1016/0378-4347(91)80241-4

https://api.elsevier.com/content/article/PII:0378434791802414?httpAccept=text/plain

28 October 2022

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1016/0378-4347(91)80241-4

Journal of Chromatography

28 October 2022

published in

569

1-2

421–47

13 September 1991

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1682336

28 October 2022

volume

569

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

page(s)

421-447

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json

The linear arrangement of six sex-linked factors in Drosophila, as shown by their mode of association

23 September 2019

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The Linkage between the Genes for Colour-Blindness and Haemophilia in Man

28 October 2022

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

28 October 2022

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Hypervariable 'minisatellite' regions in human DNA.

28 October 2022

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Variable number of tandem repeat (VNTR) markers for human gene mapping

28 October 2022

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Highly variable regions of DNA flank the human alpha globin genes

28 October 2022

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A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

28 October 2022

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An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene

28 October 2022

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A polymorphic CACA repeat in the 3' untranslated region of dystrophin.

28 October 2022

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The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome

28 October 2022

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

28 October 2022

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An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

28 October 2022

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Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

28 October 2022

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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

28 October 2022

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Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis

28 October 2022

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Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations

28 October 2022

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Parameters affecting the yield of DNA from human blood

28 October 2022

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DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA

28 October 2022

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DNA analysis in the diagnosis of hemoglobin disorders

28 October 2022

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DNA extraction with organic solvents in gel barrier tubes.

28 October 2022

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A simple salting out procedure for extracting DNA from human nucleated cells

28 October 2022

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First-trimester fetal diagnosis for haemoglobinopathies: three cases

28 October 2022

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Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA banking

28 October 2022

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Extraction of cellular DNA from human cells and tissues fixed in ethanol

28 October 2022

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Purification of DNA from formaldehyde fixed and paraffin embedded human tissue

28 October 2022

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DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screening

28 October 2022

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Vacuum blotting enhances nucleic acid transfer

28 October 2022

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Heterogeneity of the ribosomal genes in mice and men

28 October 2022

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

28 October 2022

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Rapid transfer of DNA from agarose gels to nylon membranes

28 October 2022

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

28 October 2022

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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

28 October 2022

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

28 October 2022

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Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate

28 October 2022

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Prenatal diagnosis in Becker muscular dystrophy

28 October 2022

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The rate of spontaneous mutation of a human gene

28 October 2022

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Germinal mosaicism in Duchenne muscular dystrophy

28 October 2022

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DNA polymorphism and molecular pathology of the human globin gene clusters

28 October 2022

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Detection of sickle cell anaemia and thalassaemias

28 October 2022

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Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome

28 October 2022

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

28 October 2022

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Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

28 October 2022

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Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification

28 October 2022

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Improved diagnosis of Duchenne/Becker muscular dystrophy

28 October 2022

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The mutation and polymorphism of the human beta-globin gene and its surrounding DNA.

28 October 2022

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The molecular basis of hemophilia A in man.

28 October 2022

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Haemophilia B: database of point mutations and short additions and deletions

28 October 2022

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Partial deletion of the β-globin gene: a common β-thalassaemia allele in Asian Indians

28 October 2022

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The CpG dinucleotide and human genetic disease

28 October 2022

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Modification of enzymatically amplified DNA for the detection of point mutations.

28 October 2022

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Prenatal diagnosis of beta-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes

28 October 2022

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Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA

28 October 2022

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

28 October 2022

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Detection of delta F508 deletion by amplification refractory mutation system

28 October 2022

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Detection of specific DNA sequences by fluorescence amplification: a color complementation assay

28 October 2022

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The ligation amplification reaction (LAR)--amplification of specific DNA sequences using sequential rounds of template-dependent ligation

28 October 2022

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[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis

28 October 2022

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Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes

28 October 2022

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Use of denaturing gradient gel electrophoresis to detect point mutations in the factor VIII gene

28 October 2022

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Direct detection of point mutations by mismatch analysis: application to haemophilia B.

28 October 2022

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Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

28 October 2022

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Molecular genetics in the National Health Service in Britain.

28 October 2022

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Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA banking

28 October 2022

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28 October 2022

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1682336%20AND%20SRC:MED&resulttype=core&format=json