Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1994 | 1 |
1997 | 1 |
2024 | 0 |
PubMed for id: 2490
3 results
Results by year
Filters applied: . Clear all
Page 1
Further exclusion of FSHD1B from the telomeric region of 10q.
Neurogenetics. 1997 Sep;1(2):151-2. doi: 10.1007/s100480050023.
Neurogenetics. 1997.
PMID: 10732819
Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD).
Gilbert JR, Stajich JM, Wall S, Carter SC, Qiu H, Vance JM, Stewart CS, Speer MC, Pufky J, Yamaoka LH, et al.
Gilbert JR, et al.
Am J Hum Genet. 1993 Aug;53(2):401-8.
Am J Hum Genet. 1993.
PMID: 8328457
Free PMC article.
Item in Clipboard
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD).
Cacurri S, Deidda G, Piazzo N, Novelletto A, La Cesa I, Servidei S, Galluzzi G, Wijmenga C, Frants RR, Felicetti L.
Cacurri S, et al.
Hum Genet. 1994 Oct;94(4):367-74. doi: 10.1007/BF00201595.
Hum Genet. 1994.
PMID: 7927331
Item in Clipboard
Cite
Cite