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Article

Further exclusion of FSHD1B from the telomeric region of 10q.

Neurogenetics - 1 Sept 1997

Speer M C, Pericak-Vance M A, Stajich J M, Sarrica J, Jordan M, Roses A D, Vance J M, Gilbert J R

Abstract excerpt

The localization of the gene for the majority of cases of facioscapulohumeral muscular dystrophy is established as 4q35-qter (FSHD1A), although locus heterogeneity has been demonstrated with a minority of families unlinked to 4q. In FSHD1A, the disease is associated with a deletion of 3.3 kb repeats from a tandem repeat located near the as-yet-unidentified gene. This repeat cross-hybridizes with a telomeric...

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PMID: 10732819
DOI: 10.1007/s100480050023

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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Research trail→

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Further exclusion of FSHD1B from the telomeric region of 10q.PMID 10732819Read ↗

The FSHD-linked locus D4F104S1 (p13E-11) ON 4q35 has a homologue on 10qterSemantic proximity Read ↗

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.Semantic proximity Read ↗

The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.Semantic proximity Read ↗

A Functional Role for 4qA/B in the Structural Rearrangement of the 4q35 Region and in the Regulation of FRG1 and ANT1 in Facioscapulohumeral DystrophySemantic proximity Read ↗

Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

Improved characterization of FSHD mutations.Semantic proximity Read ↗

Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

FSH dystrophy and a subtelomeric 4q haplotype: a new assay and associations with disease.Semantic proximity Read ↗

D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection.Semantic proximity Read ↗

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1Semantic proximity Read ↗

Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotype in correlation to the concurrence of 4q35 and 10q26 fragments.Semantic proximity Read ↗

Genetic mapping of human heart-skeletal muscle adenine nucleotide translocator and its relationship to the facioscapulohumeral muscular dystrophy locus.Semantic proximity Read ↗

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