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Journal Abstract Search

148 related items for PubMed ID: 9889004

  • 1.
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  • 2. A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.
    Machado RD, Pauciulo MW, Fretwell N, Veal C, Thomson JR, Vilariño Güell C, Aldred M, Brannon CA, Trembath RC, Nichols WC.
    Genomics; 2000 Sep 01; 68(2):220-8. PubMed ID: 10964520
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  • 3. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.
    Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C.
    Nat Genet; 1994 Jul 01; 7(3):425-8. PubMed ID: 7920663
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  • 4. Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.
    Hadano S, Yanagisawa Y, Skaug J, Fichter K, Nasir J, Martindale D, Koop BF, Scherer SW, Nicholson DW, Rouleau GA, Ikeda J, Hayden MR.
    Genomics; 2001 Jan 15; 71(2):200-13. PubMed ID: 11161814
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  • 7. Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33.
    Hosler BA, Sapp PC, Berger R, O'Neill G, Bejaoui K, Hamida MB, Hentati F, Chin W, McKenna-Yasek D, Haines JL, Patterson D, Horvitz HR, Brown RH, Day CB.
    Neurogenetics; 1998 Dec 15; 2(1):34-42. PubMed ID: 9933298
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  • 8. A 11 Mb YAC-based contig spanning the familial juvenile nephronophthisis region (NPH1) located on chromosome 2q.
    Konrad M, Saunier S, Silbermann F, Benessy F, Le Paslier D, Weissenbach J, Broyer M, Gubler MC, Antignac C.
    Genomics; 1995 Dec 10; 30(3):514-20. PubMed ID: 8825638
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  • 9. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.
    Engert JC, Doré C, Mercier J, Ge B, Bétard C, Rioux JD, Owen C, Bérubé P, Devon K, Birren B, Melançon SB, Morgan K, Hudson TJ, Richter A.
    Genomics; 1999 Dec 01; 62(2):156-64. PubMed ID: 10610707
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  • 10. A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.
    Kuhlenbäumer G, Schirmacher A, Meuleman J, Tissir F, Del-Favero J, Stögbauer F, Young P, Ringelstein B, Van Broeckhoven C, Timmerman V.
    Genomics; 1999 Dec 01; 62(2):242-50. PubMed ID: 10610718
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  • 11. An EST and STS-based YAC contig map of human chromosome 9q22.3.
    Lench NJ, Telford EA, Andersen SE, Moynihan TP, Robinson PA, Markham AF.
    Genomics; 1996 Dec 01; 38(2):199-205. PubMed ID: 8954802
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  • 12. Physical map of the region surrounding the OTOFERLIN locus on chromosome 2p22-p23.
    Yasunaga S, Petit C.
    Genomics; 2000 May 15; 66(1):110-2. PubMed ID: 10843812
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  • 13. A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene.
    Irobi J, Tissir F, De Jonghe P, De Vriendt E, Van Broeckhoven C, Timmerman V, Beuten J.
    Genomics; 2000 Apr 01; 65(1):34-43. PubMed ID: 10777663
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  • 14. A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6.
    Park JH, Dixit MP, Onuchic LF, Wu G, Goncharuk AN, Kneitz S, Santarina LB, Hayashi T, Avner ED, Guay-Woodford L, Zerres K, Germino GG, Somlo S.
    Genomics; 1999 Apr 15; 57(2):249-55. PubMed ID: 10198164
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  • 15. An integrated somatic cell hybrid, YAC, and BAC map of the Rmc1 region of mouse chromosome 1.
    Hunter K, Greenwood J, Yang YL, Cunningham JM, Birren B, Housman D.
    Genomics; 1999 Jun 15; 58(3):318-22. PubMed ID: 10373331
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  • 16. A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11.
    Lamartine J, Pitaval A, Soularue P, Lanneluc I, Lemaître G, Kibar Z, Rouleau GA, Waksman G.
    Genomics; 2000 Jul 15; 67(2):232-6. PubMed ID: 10903849
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  • 17. An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobin.
    Game L, Close J, Stephens P, Mitchell J, Best S, Rochette J, Louis-dit-Sully C, Riley J, See CG, Sanseau P, Kearney L, Bethel G, Humphray S, Dunham I, Mungall A, Thein SL.
    Genomics; 2000 Mar 15; 64(3):264-76. PubMed ID: 10756094
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  • 18. Novel genes mapping to the critical region of the 5q- syndrome.
    Boultwood J, Fidler C, Soularue P, Strickson AJ, Kostrzewa M, Jaju RJ, Cotter FE, Fairweather N, Monaco AP, Müller U, Lovett M, Jabs EW, Auffray C, Wainscoat JS.
    Genomics; 1997 Oct 01; 45(1):88-96. PubMed ID: 9339364
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  • 19. Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes.
    Kirschner LS, Taymans SE, Pack S, Pak E, Pike BL, Chandrasekharappa SC, Zhuang Z, Stratakis CA.
    Genomics; 1999 Nov 15; 62(1):21-33. PubMed ID: 10585764
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  • 20. Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21.
    Kärrman C, Bäckman B, Dixon M, Holmgren G, Forsman K.
    Genomics; 1997 Jan 15; 39(2):164-70. PubMed ID: 9027503
    [Abstract] [Full Text] [Related]

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