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Report of the fourth international workshop on human chromosome 11 mapping 1994.
PMID: 7698003 [PubMed - indexed for MEDLINE]
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Cited by 4 PubMed Central articles
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Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.
Iyengar S, Kalinsky H, Weiss S, Korostishevsky M, Sadeh M, Zhao Y, Kidd KK, Bonne-Tamir B.
J Med Genet. 1997 May; 34(5):391-4.
[J Med Genet. 1997]
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A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, et al.
Am J Hum Genet. 1997 May; 60(5):1168-73.
[Am J Hum Genet. 1997]
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Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene Group.
Norman RA, Thompson DB, Foroud T, Garvey WT, Bennett PH, Bogardus C, Ravussin E.
Am J Hum Genet. 1997 Jan; 60(1):166-73.
[Am J Hum Genet. 1997]
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