Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene
about
Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.Sequence-specific DNA purification by triplex affinity capture.Automated analysis of multiplex microsatellites.Determination of Duchenne muscular dystrophy carrier status by single strand conformation polymorphism analysis of deleted regions of the dystrophin locus.Parental origin of the X chromosome in a patient with a Robertsonian translocation and Turner's syndromeMale neonatal death and progressive weakness and immune deficiency in females: an unknown X linked condition.Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.Ruler arrays reveal haploid genomic structural variation.The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusFluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophyCarrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphismsNonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombinationX-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.A larger spectrum of intragenic short tandem repeats improves linkage analysis and localization of intragenic recombination detection in the dystrophin gene: an analysis of 93 families from southern Italy.Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.Heterogeneity analysis in 40 X-linked retinitis pigmentosa familiesToward fully automated genotyping: allele assignment, pedigree construction, phase determination, and recombination detection in Duchenne muscular dystrophyGenetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa.Delineation of the dystonia-parkinsonism syndrome locus in Xq13.Serum Levels of MicroRNA-206 and Novel Mini-STR Assays for Carrier Detection in Duchenne Muscular Dystrophy.A rapid method to isolate (GT)n repeats from yeast artificial chromosomes.A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD).Informative microsatellite markers allow carrier detection in a Duchenne muscular dystrophy deletion pedigree in the absence of DNA from an affected boy.
P2860
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P2860
Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene
description
1991 nî lūn-bûn
@nan
1991 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի մարտին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Rapid detection of CA polymorp ...... region of the dystrophin gene
@ast
Rapid detection of CA polymorp ...... region of the dystrophin gene
@en
type
label
Rapid detection of CA polymorp ...... region of the dystrophin gene
@ast
Rapid detection of CA polymorp ...... region of the dystrophin gene
@en
prefLabel
Rapid detection of CA polymorp ...... region of the dystrophin gene
@ast
Rapid detection of CA polymorp ...... region of the dystrophin gene
@en
P2093
P2860
P1476
Rapid detection of CA polymorp ...... region of the dystrophin gene
@en
P2093
P2860
P304
P407
P577
1991-03-01T00:00:00Z