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PUBMED FOR HANDHELDS

Journal Abstract Search

67 related items for PubMed ID: 8252033

  • 1. Homozygosity mapping: familiarity breeds debility.
    Farrall M.
    Nat Genet; 1993 Oct; 5(2):107-8. PubMed ID: 8252033
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  • 4. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
    Finckh U, Xu S, Kumaramanickavel G, Schürmann M, Mukkadan JK, Fernandez ST, John S, Weber JL, Denton MJ, Gal A.
    Genomics; 1998 Mar 15; 48(3):341-5. PubMed ID: 9545639
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  • 5. Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31.
    Lagier-Tourenne C, Tranebaerg L, Chaigne D, Gribaa M, Dollfus H, Silvestri G, Bétard C, Warter JM, Koenig M.
    Eur J Hum Genet; 2003 Oct 15; 11(10):770-8. PubMed ID: 14512967
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  • 6. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
    Hand CK, Harmon DL, Kennedy SM, FitzSimon JS, Collum LM, Parfrey NA.
    Genomics; 1999 Oct 01; 61(1):1-4. PubMed ID: 10512674
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  • 7. Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23.
    Bomont P, Watanabe M, Gershoni-Barush R, Shizuka M, Tanaka M, Sugano J, Guiraud-Chaumeil C, Koenig M.
    Eur J Hum Genet; 2000 Dec 01; 8(12):986-90. PubMed ID: 11175288
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  • 10. Homozygosity mapping and Friedreich's ataxia.
    Clarke A.
    Lancet; 1988 May 21; 1(8595):1168. PubMed ID: 2896989
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  • 11. Localisation of a Fanconi anaemia gene to chromosome 9p.
    Saar K, Schindler D, Wegner RD, Reis A, Wienker TF, Hoehn H, Joenje H, Sperling K, Digweed M.
    Eur J Hum Genet; 1998 May 21; 6(5):501-8. PubMed ID: 9801875
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  • 13. Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11.
    De Sandre-Giovannoli A, Delague V, Hamadouche T, Chaouch M, Krahn M, Boccaccio I, Maisonobe T, Chouery E, Jabbour R, Atweh S, Grid D, Mégarbané A, Lévy N.
    J Med Genet; 2005 Mar 21; 42(3):260-5. PubMed ID: 15744041
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  • 15. [Application of homozygosity mapping to the fine mapping of the osteoporosis-pseudoglioma syndrome locus].
    Gong YQ, Li JX, Liu QJ, Chen BX, Guo CH, Gao GM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Feb 21; 20(1):53-5. PubMed ID: 12579502
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  • 16. Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2.
    Faivre L, Mégarbané A, Alswaid A, Zylberberg L, Aldohayan N, Campos-Xavier B, Bacq D, Legeai-Mallet L, Bonaventure J, Munnich A, Cormier-Daire V.
    Hum Genet; 2002 Apr 21; 110(4):366-70. PubMed ID: 11941487
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  • 17. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.
    Pollak MR, Chou YH, Cerda JJ, Steinmann B, La Du BN, Seidman JG, Seidman CE.
    Nat Genet; 1993 Oct 21; 5(2):201-4. PubMed ID: 8252048
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  • 20. Computation of multilocus prior probability of autozygosity for complex inbred pedigrees.
    Guo SW.
    Genet Epidemiol; 1997 Oct 21; 14(1):1-15. PubMed ID: 9055058
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