Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes

scientific article

Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1136/JMG.27.5.292
P932PMC publication ID1017078
P698PubMed publication ID2191136
P5875ResearchGate publication ID20965195

P2093author name stringMorris A
Ferguson-Smith MA
Connor JM
Cooke A
Wilcox DE
Lanyon WG
Kataki A
McWhinnie AJ
Dornan ES
Gillard EF
P2860cites workThe complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinQ28118471
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsQ30050310
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutQ35247811
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patientsQ36120575
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophyQ36423501
Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletionQ37541303
Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic markerQ43752749
Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.Q52078680
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.Q54789059
Preferential deletion of exons in Duchenne and Becker muscular dystrophiesQ59065476
Molecular deletion patterns in Duchenne and Becker type muscular dystrophyQ69737086
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophyQ69896114
A deletion hot spot in the Duchenne muscular dystrophy geneQ69922944
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectBecker muscular dystrophyQ2484592
P304page(s)292-297
P577publication date1990-05-01
P1433published inJournal of Medical GeneticsQ14640281
P1476titleAnalysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes
P478volume27

Reverse relations

cites work (P2860)
Q72067856A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intron
Q33596646Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene
Q42063901Deletion patterns of Duchenne and Becker muscular dystrophies in Greece
Q78048699High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling
Q33595755Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups
Q52862565Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study.
Q44534260Patterns of deletions of the dystrophin gene in different European populations
Q33594787Quantitative Southern blot analysis in the dystrophin gene of Japanese patients with Duchenne or Becker muscular dystrophy: a high frequency of duplications
Q33593754Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients
Q52041951Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population.