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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

115 related items for PubMed ID: 7635931

  • 1.
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  • 2. Genetic linkage studies with cleft lip and palate: report of two family studies.
    Spence MA, Glass L, Crandall BF, Stewart RE, Miles J, Falk RE, Field LL, Sparkes RS.
    J Craniofac Genet Dev Biol; 1983; 3(3):207-12. PubMed ID: 6580294
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  • 3. Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
    Zeiger JS, Hetmanski JB, Beaty TH, VanderKolk CA, Wyszynski DF, Bailey-Wilson JE, de Luna RO, Perandones C, Tolarova MM, Mosby T, Bennun R, Segovia M, Calda P, Pugh EW, Doheny K, McIntosh I.
    Eur J Hum Genet; 2003 Nov; 11(11):835-9. PubMed ID: 14571267
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  • 4. Linkage analysis of candidate endothelin pathway genes in nonsyndromic familial orofacial cleft.
    Pezzetti F, Scapoli L, Martinelli M, Carinci F, Brunelli G, Carls FP, Palomba F, Gombos F, Carinci P, Tognon M.
    Ann Hum Genet; 2000 Jul; 64(Pt 4):341-7. PubMed ID: 11415518
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  • 5. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S.
    Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
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  • 6. Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate.
    Scapoli L, Martinelli M, Pezzetti F, Carinci F, Bodo M, Tognon M, Carinci P.
    Hum Genet; 2002 Jan; 110(1):15-20. PubMed ID: 11810291
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  • 7. Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.
    Beiraghi S, Miller-Chisholm A, Kimberling WJ, Sun CE, Wang YF, Russell LJ, Khoshnevisan M, Storm AL, Long RE, Witt PD, Mazaheri M, Diehl SR.
    J Craniofac Genet Dev Biol; 1999 Jan; 19(3):128-34. PubMed ID: 10589394
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  • 9. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
    Griffith AJ, Burgess DL, Kohrman DC, Yu J, Blaschak J, Blanton SH, Boehnke M, Hecht JT, Overhauser J, Meisler MH.
    Genomics; 1996 Jun 15; 34(3):299-303. PubMed ID: 8786128
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  • 13. Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3.
    Donnai D, Heather LJ, Sinclair P, Thakker Y, Scambler PJ, Dixon MJ.
    Clin Dysmorphol; 1992 Apr 15; 1(2):89-97. PubMed ID: 1345518
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  • 17. Genetic analysis of cleft lip with or without cleft palate in Danish kindreds.
    Marazita ML, Spence MA, Melnick M.
    Am J Med Genet; 1984 Sep 15; 19(1):9-18. PubMed ID: 6496575
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  • 18. Genomic scan for genes predisposing to schizophrenia.
    Coon H, Jensen S, Holik J, Hoff M, Myles-Worsley M, Reimherr F, Wender P, Waldo M, Freedman R, Leppert M.
    Am J Med Genet; 1994 Mar 15; 54(1):59-71. PubMed ID: 7909992
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  • 19. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.
    Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M, Park N, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Knowles JA, Ott J, Gilliam TC, Baron M.
    Mol Psychiatry; 2003 Mar 15; 8(3):333-42. PubMed ID: 12660806
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  • 20. Genetic analysis of the construction of the AEJ.A congenic strain indicates that nonsyndromic CL(P) in the mouse is caused by two loci with epistatic interaction.
    Juriloff DM.
    J Craniofac Genet Dev Biol; 1995 Mar 15; 15(1):1-12. PubMed ID: 7601909
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