Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
about
Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy geneMolecular cloning of the human esterase D gene, a genetic marker of retinoblastomaDeletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndromeFine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21Attempting to Compensate for Reduced Neuronal Nitric Oxide Synthase Protein with Nitrate Supplementation Cannot Overcome Metabolic Dysfunction but Rather Has Detrimental Effects in Dystrophin-Deficient mdx Muscle.Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy.Linkage analysis of X linked retinitis pigmentosa in the Irish population.Benign muscular dystrophy: risk calculation in families with consanguinity.Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients.Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation.Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11.Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy geneScreening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study.Muscular dystrophy in girls with X;autosome translocations.Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyMolecular 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 studies in Duchenne and Becker muscular dystrophies.Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyPrenatal diagnosis of Duchenne muscular dystrophy by DNA analysisCarrier 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.The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.Partial gene duplication in Duchenne and Becker muscular dystrophies.Inherited deletion of subband Xp21.13 in a male with Duchenne muscular dystrophy.Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMDEmerging genetic therapies to treat Duchenne muscular dystrophyDNA analysis in human diseaseA yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene2004 William Allan Award address. Cloning of the DMD gene.Improved diagnosis of Duchenne/Becker muscular dystrophyIsolating the gene for Duchenne muscular dystrophy.Searching for candidate genes in the new millennium.Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.Evolution of homologous sequences on the human X and Y chromosomes, outside of the meiotic pairing segment.A 230kb cosmid walk in the Duchenne muscular dystrophy gene: detection of a conserved sequence and of a possible deletion prone region.
P2860
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P2860
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh
1985年學術文章
@zh-hant
name
Detection of deletions spannin ...... a tightly linked DNA segment.
@ast
Detection of deletions spannin ...... a tightly linked DNA segment.
@en
type
label
Detection of deletions spannin ...... a tightly linked DNA segment.
@ast
Detection of deletions spannin ...... a tightly linked DNA segment.
@en
prefLabel
Detection of deletions spannin ...... a tightly linked DNA segment.
@ast
Detection of deletions spannin ...... a tightly linked DNA segment.
@en
P2093
P356
P1433
P1476
Detection of deletions spannin ...... a tightly linked DNA segment.
@en
P2093
Aldridge J
Bartlett R
Bertelson CJ
Colletti CA
Fischbeck KH
Middlesworth W
Pericak-Vance MA
P2888
P304
P356
10.1038/316842A0
P407
P577
1985-08-01T00:00:00Z
P5875
P6179
1043744101