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Journal Abstract Search

179 related items for PubMed ID: 7493033

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  • 3. Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
    McDonald-McGinn DM, Driscoll DA, Bason L, Christensen K, Lynch D, Sullivan K, Canning D, Zavod W, Quinn N, Rome J.
    Am J Med Genet; 1995 Oct 23; 59(1):103-13. PubMed ID: 8849001
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  • 6. The G and BBB syndromes: case presentations, genetics, and nosology.
    Funderburk SJ, Stewart R.
    Am J Med Genet; 1978 Oct 23; 2(2):131-44. PubMed ID: 263433
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  • 9. Opitz GBBB syndrome and the 22q11.2 deletion.
    Lacassie Y, Arriaza MI.
    Am J Med Genet; 1996 Mar 29; 62(3):318. PubMed ID: 8882795
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  • 10. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.
    Diaz GA, Khan KT, Gelb BD.
    Genomics; 1998 Nov 15; 54(1):13-8. PubMed ID: 9806825
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  • 11. Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndrome.
    Stoll C, Geraudel A, Berland H, Roth MP, Dott B.
    Am J Med Genet; 1985 Feb 15; 20(2):221-5. PubMed ID: 4038851
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  • 14. Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.
    Stine OC, McMahon FJ, Chen L, Xu J, Meyers DA, MacKinnon DF, Simpson S, McInnis MG, Rice JP, Goate A, Reich T, Edenberg HJ, Foroud T, Nurnberger JI, Detera-Wadleigh SD, Goldin LR, Guroff J, Gershon ES, Blehar MC, DePaulo JR.
    Am J Med Genet; 1997 May 31; 74(3):263-9. PubMed ID: 9184308
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  • 15. G syndrome: an unusual family.
    Allanson JE.
    Am J Med Genet; 1988 Nov 31; 31(3):637-42. PubMed ID: 3228142
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  • 20. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.
    Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF.
    Hum Mol Genet; 2006 Jan 15; 15(2):251-8. PubMed ID: 16330481
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