Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.
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The major human erythroid DNA-binding protein (GF-1): primary sequence and localization of the gene to the X chromosomeContiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeDeletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophreniaMolecular physiology of weight regulation in mice and humansDown-regulation of a novel actin-binding molecule, skeletrophin, in malignant melanomaIdentification of human renal cell carcinoma associated genes by suppression subtractive hybridizationCorrelation of clinical and deletion data in Duchenne and Becker muscular dystrophy.Subtracted, unique-sequence, in situ hybridization: experimental and diagnostic applicationsCoincidence cloning of Alu PCR products.Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries.Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.Linkage analysis of X linked retinitis pigmentosa in the Irish population.Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11.Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophyAnalysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.Muscular dystrophy in girls with X;autosome translocations.Molecular deletion analysis in Duchenne muscular dystrophy.The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy familiesLinkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyCarrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.Inherited deletion of subband Xp21.13 in a male with Duchenne muscular dystrophy.The value of the study of natural history in genetic disorders and congenital anomaly syndromes.Linkage of a medium sized Scottish autosomal dominant retinitis pigmentosa family to chromosome 7q.The golden retriever model of Duchenne muscular dystrophy.The muscular dystrophies.2004 William Allan Award address. Cloning of the DMD gene.Isolation of the Ascobolus immersus spore color gene b2 and study in single cells of gene silencing by methylation induced premeiotically.Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region.Functional correction of adult mdx mouse muscle using gutted adenoviral vectors expressing full-length dystrophin.Inefficient dystrophin expression after cord blood transplantation in Duchenne muscular dystrophy.Isolating the gene for Duchenne muscular dystrophy.Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardationCongenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.Gene replacement therapies for duchenne muscular dystrophy using adeno-associated viral vectors.The electron transport chain of the microbicidal oxidase of phagocytic cells and its involvement in the molecular pathology of chronic granulomatous disease.Evolution of homologous sequences on the human X and Y chromosomes, outside of the meiotic pairing segment.Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.
P2860
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P2860
Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 1985
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Specific cloning of DNA fragme ...... with an X chromosome deletion.
@en
Specific cloning of DNA fragme ...... with an X chromosome deletion.
@nl
type
label
Specific cloning of DNA fragme ...... with an X chromosome deletion.
@en
Specific cloning of DNA fragme ...... with an X chromosome deletion.
@nl
prefLabel
Specific cloning of DNA fragme ...... with an X chromosome deletion.
@en
Specific cloning of DNA fragme ...... with an X chromosome deletion.
@nl
P2093
P2860
P356
P1476
Specific cloning of DNA fragme ...... with an X chromosome deletion.
@en
P2093
L M Kunkel
W Middlesworth
P2860
P304
P356
10.1073/PNAS.82.14.4778
P407
P577
1985-07-01T00:00:00Z