Further exclusion of FSHD1B from the telomeric region of 10q.
Publication
, Journal Article
Speer, MC; Pericak-Vance, MA; Stajich, JM; Sarrica, J; Jordan, M; Roses, AD; Vance, JM; Gilbert, JR
Published in: Neurogenetics
September 1997
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 region on 10q, making this cross-hybridizing region a feasible candidate gene for FSHD1B. We have tested the most telomeric marker on 10q (sAVA4) and excluded approximately 17 cM on either side of this marker as harboring the FSHD1B gene.
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Published In
Neurogenetics
DOI
ISSN
1364-6745
Publication Date
September 1997
Volume
1
Issue
2
Start / End Page
151 / 152
Location
United States
Related Subject Headings
- Telomere
- Pedigree
- Neurology & Neurosurgery
- Muscular Dystrophy, Facioscapulohumeral
- Microsatellite Repeats
- Male
- Lod Score
- Humans
- Genotype
- Genetic Predisposition to Disease
Citation
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ICMJE
MLA
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Speer, M. C., Pericak-Vance, M. A., Stajich, J. M., Sarrica, J., Jordan, M., Roses, A. D., … Gilbert, J. R. (1997). Further exclusion of FSHD1B from the telomeric region of 10q. Neurogenetics, 1(2), 151–152. https://doi.org/10.1007/s100480050023
Speer, M. C., M. A. Pericak-Vance, J. M. Stajich, J. Sarrica, M. Jordan, A. D. Roses, J. M. Vance, and J. R. Gilbert. “Further exclusion of FSHD1B from the telomeric region of 10q.” Neurogenetics 1, no. 2 (September 1997): 151–52. https://doi.org/10.1007/s100480050023.
Speer MC, Pericak-Vance MA, Stajich JM, Sarrica J, Jordan M, Roses AD, et al. Further exclusion of FSHD1B from the telomeric region of 10q. Neurogenetics. 1997 Sep;1(2):151–2.
Speer, M. C., et al. “Further exclusion of FSHD1B from the telomeric region of 10q.” Neurogenetics, vol. 1, no. 2, Sept. 1997, pp. 151–52. Pubmed, doi:10.1007/s100480050023.
Speer MC, Pericak-Vance MA, Stajich JM, Sarrica J, Jordan M, Roses AD, Vance JM, Gilbert JR. Further exclusion of FSHD1B from the telomeric region of 10q. Neurogenetics. 1997 Sep;1(2):151–152.
Published In
Neurogenetics
DOI
ISSN
1364-6745
Publication Date
September 1997
Volume
1
Issue
2
Start / End Page
151 / 152
Location
United States
Related Subject Headings
- Telomere
- Pedigree
- Neurology & Neurosurgery
- Muscular Dystrophy, Facioscapulohumeral
- Microsatellite Repeats
- Male
- Lod Score
- Humans
- Genotype
- Genetic Predisposition to Disease