(Q44434211)

2 December 2017

title

Applications and limitations of direct DNA analysis in genetic prediction (English)

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nucleic acid sequence analysis

2 December 2017

main subject

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M E Pembrey

1

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2 December 2017

publication date

1 January 1986

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Journal of Inherited Metabolic Disease

2 December 2017

published in

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2 December 2017

volume

9 Suppl 1

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2 December 2017

page(s)

38-48

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https://scigraph.springernature.com/pub.10.1007/bf01800857

2 December 2017

exact match

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cites work

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

1 reference

12 December 2020

Antenatal diagnosis and carrier detection of haemophilia A using factor VIII gene probe

1 reference

12 December 2020

Plasma assay of fetal factors VIIIC and IX for prenatal diagnosis of haemophilia

1 reference

12 December 2020

Hypervariable 'minisatellite' regions in human DNA.

1 reference

12 December 2020

1 reference

12 December 2020

Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients

1 reference

12 December 2020

Polymorphism and molecular pathology of the human beta-globin gene

1 reference

12 December 2020

Direct vision chorion biopsy and chromosome-specific DNA probes for determination of fetal sex in first-trimester prenatal diagnosis

1 reference

12 December 2020

Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

1 reference

12 December 2020

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

12 December 2020

Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis

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12 December 2020

A clinically useful DNA probe closely linked to haemophilia A

1 reference

12 December 2020

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

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12 December 2020

A Sensitive New Prenatal Test for Sickle-Cell Anemia

1 reference

12 December 2020

Characterization of the human factor VIII gene

1 reference

12 December 2020

First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13.

1 reference

12 December 2020

Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locus

1 reference

12 December 2020

Immunologic studies of factor VIII coagulant activity (VIII:C) 1. Assays based on a haemophilic and an acquired antibody to VIII:C.

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe

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12 December 2020

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

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12 December 2020

Genotype assignment (carrier detection) in the haemophilias

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12 December 2020

Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiency

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12 December 2020

Identifiers

DOI

10.1007/BF01800857

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2 December 2017

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