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The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
Genomics. 1997 Feb 15;40(1):73-9. doi: 10.1006/geno.1996.4545.
Genomics. 1997.
PMID: 9070921
Free article.
The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41.
Sumegi J, Wang JY, Zhen DK, Eudy JD, Talmadge CB, Li BF, Berglund P, Weston MD, Yao SF, Ma-Edmonds M, Overbeck L, Kelley PM, Zabarovsky E, Uzvolgyi E, Stanbridge EJ, Klein G, Kimberling WJ.
Sumegi J, et al.
Genomics. 1996 Jul 1;35(1):79-86. doi: 10.1006/geno.1996.0325.
Genomics. 1996.
PMID: 8661107
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Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
Weston MD, Kelley PM, Overbeck LD, Wagenaar M, Orten DJ, Hasson T, Chen ZY, Corey D, Mooseker M, Sumegi J, Cremers C, Moller C, Jacobson SG, Gorin MB, Kimberling WJ.
Weston MD, et al. Among authors: overbeck ld.
Am J Hum Genet. 1996 Nov;59(5):1074-83.
Am J Hum Genet. 1996.
PMID: 8900236
Free PMC article.
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A new highly polymorphic dinucleotide (CT)n repeat polymorphism D1S158 on chromosome 1q isolated by microdissection.
Overbeck LD, Weston MD, Kimberling WJ, Johnson DH.
Overbeck LD, et al.
Hum Mol Genet. 1992 May;1(2):141. doi: 10.1093/hmg/1.2.141.
Hum Mol Genet. 1992.
PMID: 1301158
No abstract available.
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Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR).
Dahl SP, Weston MD, Overbeck LD, Evans KL, Porteous DJ, Kimberling WJ.
Dahl SP, et al. Among authors: overbeck ld.
Hum Mol Genet. 1993 Jun;2(6):822. doi: 10.1093/hmg/2.6.822-a.
Hum Mol Genet. 1993.
PMID: 8353507
No abstract available.
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Dinucleotide (CT)n (CA)n repeat polymorphism for D11S787 on chromosome 11q13.4.
Overbeck LD, Weston MD, Kimberling WJ, Evans GA.
Overbeck LD, et al.
Hum Mol Genet. 1993 May;2(5):611. doi: 10.1093/hmg/2.5.611.
Hum Mol Genet. 1993.
PMID: 8518805
No abstract available.
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Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ.
Abe S, et al. Among authors: overbeck ld.
Eur J Hum Genet. 1998 Nov-Dec;6(6):563-9. doi: 10.1038/sj.ejhg.5200239.
Eur J Hum Genet. 1998.
PMID: 9887373
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