Detection of novel genetic markers by mismatch analysis. - Wikidata - awgldk - TriplyDB

Detection of novel genetic markers by mismatch analysis.

Detection of novel genetic markers by mismatch analysis.

http://www.wikidata.org/entity/Q35238935

about

Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination A MaeIII polymorphism near the dystrophin gene promoter by restriction of amplified DNA Detection of single base mismatches of thymine and cytosine residues by potassium permanganate and hydroxylamine in the presence of tetralkylammonium salts.An STS in the human IL7 gene located at 8q12-13.Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles.Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

P2860

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P2860

Detection of novel genetic markers by mismatch analysis.

http://www.wikidata.org/entity/Q35238935

description

1989 nî lūn-bûn

@nan

1989 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1989 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1989年の論文

@ja

1989年論文

@yue

1989年論文

@zh-hant

1989年論文

@zh-hk

1989年論文

@zh-mo

1989年論文

@zh-tw

1989年论文

@wuu

name

Detection of novel genetic markers by mismatch analysis.

@ast

Detection of novel genetic markers by mismatch analysis.

@en

type

label

Detection of novel genetic markers by mismatch analysis.

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Detection of novel genetic markers by mismatch analysis.

@en

prefLabel

Detection of novel genetic markers by mismatch analysis.

@ast

Detection of novel genetic markers by mismatch analysis.

@en

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Nucleic Acids Research

P1476

Detection of novel genetic markers by mismatch analysis.

@en

P2093

Bentley DR

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Bobrow M

http://www.w3.org/2001/XMLSchema#string

Montandon AJ

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P2860

DNA sequencing with chain-terminating inhibitors

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

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

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

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

Molecular pathology of haemophilia B

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

The X chromosome shows less genetic variation at restriction sites than the autosomes.

A strategy to reveal high-frequency RFLPs along the human X chromosome

P304

5961-5971

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scholarly article

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10.1093/NAR/17.15.5961

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15

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17

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Roland G. Roberts

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1989-08-01T00:00:00Z

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20586571

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2570401

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