scholarly article | Q13442814 |
P2093 | author name string | Harper PS | |
Sarfarazi M | |||
Upadhyaya M | |||
Broadhead W | |||
Lunt P | |||
Farnham J | |||
P2860 | cites work | Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium | Q35195748 |
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 locus | Q40516170 | ||
A highly polymorphic VNTR locus on the long arm of chromosome 4 | Q40532107 | ||
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization | Q41688379 | ||
Recombination events suggest potential sites for the Huntington's disease gene | Q44168431 | ||
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 14 | Q68031073 | ||
DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease | Q68161008 | ||
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates | Q24679121 | ||
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 | ||
An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease | Q33593149 | ||
A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes | Q33593160 | ||
A workshop on facioscapulohumeral (Landouzy-Déjérine) disease, Manchester, 16 to 17 November 1988 | Q33593208 | ||
Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias | Q33593427 | ||
Genetic counselling in facioscapulohumeral muscular dystrophy | Q33597601 | ||
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 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | facioscapulohumeral muscular dystrophy | Q1399182 |
P304 | page(s) | 404-410 | |
P577 | publication date | 1992-08-01 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD) | |
P478 | volume | 51 |
Q35195000 | A 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). |
Q56969125 | Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD) |
Q33625003 | De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1). |
Q33681314 | Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression. |
Q92223404 | Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism |
Q33677298 | Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy |
Q64226580 | SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite |
Q46971971 | The 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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