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Journal Abstract Search

241 related items for PubMed ID: 7468659

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  • 22. A novel frameshift mutation in the EYA1 gene in a Korean family with branchio-oto-renal syndrome.
    Lee JD, Kim SC, Koh YW, Lee HJ, Choi SY, Kim UK.
    Ann Clin Lab Sci; 2009; 39(3):303-6. PubMed ID: 19667416
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  • 27. Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q.
    Wang Y, Treat K, Schroer RJ, O'Brien JE, Stevenson RE, Schwartz CE.
    Am J Med Genet; 1994 Jun 01; 51(2):169-75. PubMed ID: 8092198
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  • 32. Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred.
    Heimler A, Lieber E.
    Am J Med Genet; 1986 Sep 01; 25(1):15-27. PubMed ID: 3799714
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  • 37. Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition: branchio-oto-costal syndrome?
    Clementi M, Mammi I, Tenconi R.
    Am J Med Genet; 1997 Jan 10; 68(1):91-3. PubMed ID: 8986284
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  • 38. Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.
    Kumar S, Kimberling WJ, Lanyi A, Sumegi J, Pinnt J, Ing P, Tinley S, Marres HA, Cremers CW.
    Genomics; 1996 Jan 01; 31(1):71-9. PubMed ID: 8808282
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  • 39. Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.
    Kumar S, Deffenbacher K, Marres HA, Cremers CW, Kimberling WJ.
    Am J Hum Genet; 2000 May 01; 66(5):1715-20. PubMed ID: 10762556
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