The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)

scientific article

The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD) is …
instance of (P31):
scholarly articleQ13442814

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P932PMC publication ID1682684
P698PubMed publication ID1642238

P2093author name stringHarper PS
Sarfarazi M
Upadhyaya M
Broadhead W
Lunt P
Farnham J
P2860cites workRegional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortiumQ35195748
Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4[HGM provisional no. D4S139]Q35229005
Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.Q35843948
Dinucleotide repeat polymorphism at the D4S171 locusQ40516170
A highly polymorphic VNTR locus on the long arm of chromosome 4Q40532107
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridizationQ41688379
Recombination events suggest potential sites for the Huntington's disease geneQ44168431
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.Q55052229
Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14Q68031073
DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral diseaseQ68161008
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination ratesQ24679121
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityQ26778490
An exclusion map for facioscapulohumeral (Landouzy-Déjérine) diseaseQ33593149
A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probesQ33593160
A workshop on facioscapulohumeral (Landouzy-Déjérine) disease, Manchester, 16 to 17 November 1988Q33593208
Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment biasQ33593427
Genetic counselling in facioscapulohumeral muscular dystrophyQ33597601
Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4.Q34482812
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)Q35195742
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectfacioscapulohumeral muscular dystrophyQ1399182
P304page(s)404-410
P577publication date1992-08-01
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titleThe mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)
P478volume51

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cites work (P2860)
Q35195000A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
Q56969125Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD)
Q33625003De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).
Q33681314Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.
Q92223404Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism
Q33677298Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
Q64226580SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite
Q46971971The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

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