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Journal Abstract Search

131 related items for PubMed ID: 8288248

  • 21.
    ; . PubMed ID:
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  • 22. Linkage study of the D5 dopamine receptor gene (DRD5) in multiplex Icelandic and English schizophrenia pedigrees.
    Kalsi G, Sherrington R, Mankoo BS, Brynjolfsson J, Sigmundsson T, Curtis D, Read T, Murphy P, Butler R, Petursson H, Gurling HM.
    Am J Psychiatry; 1996 Jan; 153(1):107-9. PubMed ID: 8540565
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension.
    Thibonnier M, Graves MK, Wagner MS, Chatelain N, Soubrier F, Corvol P, Willard HF, Jeunemaitre X.
    J Mol Cell Cardiol; 2000 Apr; 32(4):557-64. PubMed ID: 10756113
    [Abstract] [Full Text] [Related]

  • 25. Transmission disequilibrium testing of dopamine-related candidate gene polymorphisms in ADHD: confirmation of association of ADHD with DRD4 and DRD5.
    Kustanovich V, Ishii J, Crawford L, Yang M, McGough JJ, McCracken JT, Smalley SL, Nelson SF.
    Mol Psychiatry; 2004 Jul; 9(7):711-7. PubMed ID: 14699430
    [Abstract] [Full Text] [Related]

  • 26. The ovine Booroola fecundity gene (FecB) is linked to markers from a region of human chromosome 4q.
    Montgomery GW, Crawford AM, Penty JM, Dodds KG, Ede AJ, Henry HM, Pierson CA, Lord EA, Galloway SM, Schmack AE.
    Nat Genet; 1993 Aug; 4(4):410-4. PubMed ID: 8401591
    [Abstract] [Full Text] [Related]

  • 27. Markers close to the dopamine D5 receptor gene (DRD5) show significant association with schizophrenia but not bipolar disorder.
    Muir WJ, Thomson ML, McKeon P, Mynett-Johnson L, Whitton C, Evans KL, Porteous DJ, Blackwood DH.
    Am J Med Genet; 2001 Mar 08; 105(2):152-8. PubMed ID: 11304828
    [Abstract] [Full Text] [Related]

  • 28.
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  • 29. A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p.
    Chen H, Kalaitsidaki M, Warren AC, Avramopoulos D, Antonarakis SE.
    Genomics; 1993 Mar 08; 15(3):621-5. PubMed ID: 8468057
    [Abstract] [Full Text] [Related]

  • 30. Polymorphic SSR (simple-sequence-repeat) markers for chromosome 20.
    Melis R, Bradley P, Elsner T, Robertson M, Lawrence E, Gerken S, Albertsen H, White R.
    Genomics; 1993 Apr 08; 16(1):56-62. PubMed ID: 8486385
    [Abstract] [Full Text] [Related]

  • 31.
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  • 32. The Booroola fecundity (FecB) gene maps to sheep chromosome 6.
    Montgomery GW, Lord EA, Penty JM, Dodds KG, Broad TE, Cambridge L, Sunden SL, Stone RT, Crawford AM.
    Genomics; 1994 Jul 01; 22(1):148-53. PubMed ID: 7959761
    [Abstract] [Full Text] [Related]

  • 33.
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  • 34. Human cholecystokinin type A receptor gene: cytogenetic localization, physical mapping, and identification of two missense variants in patients with obesity and non-insulin-dependent diabetes mellitus (NIDDM).
    Inoue H, Iannotti CA, Welling CM, Veile R, Donis-Keller H, Permutt MA.
    Genomics; 1997 Jun 01; 42(2):331-5. PubMed ID: 9192855
    [Abstract] [Full Text] [Related]

  • 35. Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci.
    Hawi Z, Lowe N, Kirley A, Gruenhage F, Nöthen M, Greenwood T, Kelsoe J, Fitzgerald M, Gill M.
    Mol Psychiatry; 2003 Mar 01; 8(3):299-308. PubMed ID: 12660802
    [Abstract] [Full Text] [Related]

  • 36. A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference.
    Zahn LM, Kwiatkowski DJ.
    Genomics; 1995 Jul 20; 28(2):140-6. PubMed ID: 8530019
    [Abstract] [Full Text] [Related]

  • 37. Twelve new polymorphic microsatellites on human chromosome 22.
    Porter JC, Ram KT, Puck JM.
    Genomics; 1993 Jan 20; 15(1):57-61. PubMed ID: 8432551
    [Abstract] [Full Text] [Related]

  • 38. Assignment of the human poly(A) polymerase (PAP) gene to chromosome 14q32.1-q32.2 and isolation of a polymorphic CA repeat sequence.
    Yamauchi T, Sugimoto J, Hatakeyama T, Asakawa S, Shimizu N, Isobe M.
    J Hum Genet; 1999 Jan 20; 44(4):253-5. PubMed ID: 10429366
    [Abstract] [Full Text] [Related]

  • 39. Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects.
    Stumpo DJ, Eddy RL, Haley LL, Sait S, Shows TB, Lai WS, Young WS, Speer MC, Dehejia A, Polymeropoulos M, Blackshear PJ.
    Genomics; 1998 Apr 15; 49(2):253-64. PubMed ID: 9598313
    [Abstract] [Full Text] [Related]

  • 40. A genetic analysis of the Werner syndrome region on human chromosome 8p.
    Thomas W, Rubenstein M, Goto M, Drayna D.
    Genomics; 1993 Jun 15; 16(3):685-90. PubMed ID: 8325642
    [Abstract] [Full Text] [Related]

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