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Journal Abstract Search

260 related items for PubMed ID: 10644429

  • 21. [Evaluation of q11-q13 locus of chromosome 15 aberrations and polymorphisms in the B3 subunit of the GABA-A receptor gene (GABRB3) in autistic patients].
    Słopień A, Rajewski A, Budny B, Czerski P.
    Psychiatr Pol; 2002; 36(5):779-91. PubMed ID: 12491987
    [Abstract] [Full Text] [Related]

  • 22. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, Yang J, Hinds D, Myers RM, Risch N.
    Am J Med Genet; 1999 Oct 15; 88(5):551-6. PubMed ID: 10490715
    [Abstract] [Full Text] [Related]

  • 23. A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 region.
    Mitsuda N, Nakura J, Ye L, Zhao Y, Fujioka Y, Takahashi-Fujii A, Ishino Y, Kato I, Hashimoto K, Ogihara T, Miki T.
    Genomics; 1997 Apr 01; 41(1):49-55. PubMed ID: 9126481
    [Abstract] [Full Text] [Related]

  • 24. Sequence-ready contig for the 1.4-cM ductal carcinoma in situ loss of heterozygosity region on chromosome 8p22-p23.
    Wang JC, Radford DM, Holt MS, Helms C, Goate A, Brandt W, Parik M, Phillips NJ, DeSchryver K, Schuh ME, Fair KL, Ritter JH, Marshall P, Donis-Keller H.
    Genomics; 1999 Aug 15; 60(1):1-11. PubMed ID: 10458905
    [Abstract] [Full Text] [Related]

  • 25. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.
    Biol Psychiatry; 2009 Aug 15; 66(4):349-59. PubMed ID: 19278672
    [Abstract] [Full Text] [Related]

  • 26. A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13.
    Cooper PR, Nowak NJ, Higgins MJ, Simpson SA, Marquardt A, Stoehr H, Weber BH, Gerhard DS, de Jong PJ, Shows TB.
    Genomics; 1997 Apr 15; 41(2):185-92. PubMed ID: 9143493
    [Abstract] [Full Text] [Related]

  • 27. Construction of a gene map of the nephronophthisis type 1 (NPHP1) region on human chromosome 2q12-q13.
    Nothwang HG, Stubanus M, Adolphs J, Hanusch H, Vossmerbäumer U, Denich D, Kübler M, Mincheva A, Lichter P, Hildebrandt F.
    Genomics; 1998 Jan 15; 47(2):276-85. PubMed ID: 9479500
    [Abstract] [Full Text] [Related]

  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. A sequence-ready physical map of the region containing the human natural killer gene complex on chromosome 12p12.3-p13.2.
    Renedo M, Arce I, Montgomery K, Roda-Navarro P, Lee E, Kucherlapati R, Fernández-Ruiz E.
    Genomics; 2000 Apr 15; 65(2):129-36. PubMed ID: 10783260
    [Abstract] [Full Text] [Related]

  • 30. A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region.
    Reid LH, Davies C, Cooper PR, Crider-Miller SJ, Sait SN, Nowak NJ, Evans G, Stanbridge EJ, deJong P, Shows TB, Weissman BE, Higgins MJ.
    Genomics; 1997 Aug 01; 43(3):366-75. PubMed ID: 9268640
    [Abstract] [Full Text] [Related]

  • 31. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
    Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS.
    Mol Psychiatry; 2003 Jun 01; 8(6):624-34, 570. PubMed ID: 12851639
    [Abstract] [Full Text] [Related]

  • 32. Physical and transcript map of the hereditary prostate cancer region at xq27.
    Stephan DA, Howell GR, Teslovich TM, Coffey AJ, Smith L, Bailey-Wilson JE, Malechek L, Gildea D, Smith JR, Gillanders EM, Schleutker J, Hu P, Steingruber HE, Dhami P, Robbins CM, Makalowska I, Carpten JD, Sood R, Mumm S, Reinbold R, Bonner TI, Baffoe-Bonnie A, Bubendorf L, Heiskanen M, Kallioneimi OP, Baxevanis AD, Joseph SS, Zucchi I, Burk RD, Isaacs W, Ross MT, Trent JM.
    Genomics; 2002 Jan 01; 79(1):41-50. PubMed ID: 11827456
    [Abstract] [Full Text] [Related]

  • 33. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME.
    Clin Genet; 2006 Feb 01; 69(2):124-34. PubMed ID: 16433693
    [Abstract] [Full Text] [Related]

  • 34. A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13.
    Guru SC, Olufemi SE, Manickam P, Cummings C, Gieser LM, Pike BL, Bittner ML, Jiang Y, Chinault AC, Nowak NJ, Brzozowska A, Crabtree JS, Wang Y, Roe BA, Weisemann JM, Boguski MS, Agarwal SK, Burns AL, Spiegel AM, Marx SJ, Flejter WL, de Jong PJ, Collins FS, Chandrasekharappa SC.
    Genomics; 1997 Jun 15; 42(3):436-45. PubMed ID: 9205115
    [Abstract] [Full Text] [Related]

  • 35. The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical map.
    Ellsworth RE, Ionasescu V, Searby C, Sheffield VC, Braden VV, Kucaba TA, McPherson JD, Marra MA, Green ED.
    Genome Res; 1999 Jun 15; 9(6):568-74. PubMed ID: 10400924
    [Abstract] [Full Text] [Related]

  • 36. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
    Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH.
    Hum Mol Genet; 1999 Jun 15; 8(6):1025-37. PubMed ID: 10332034
    [Abstract] [Full Text] [Related]

  • 37. A 1.2-megabase BAC/PAC contig spanning the 14q13 breakpoint of t(2; 14) in a mirror-image polydactyly patient.
    Matsumoto N, Soeda E, Ohashi H, Fujimoto M, Kato R, Tsujita T, Tomita H, Kondo S, Fukushima Y, Niikawa N.
    Genomics; 1997 Oct 01; 45(1):11-6. PubMed ID: 9339355
    [Abstract] [Full Text] [Related]

  • 38. Restriction map of a YAC and cosmid contig encompassing the oculopharyngeal muscular dystrophy candidate region on chromosome 14q11.2-q13.
    Xie YG, Rochefort D, Brais B, Howard H, Han FY, Gou LP, Maciel P, The BT, Larsson C, Rouleau GA.
    Genomics; 1998 Sep 01; 52(2):201-4. PubMed ID: 9782086
    [Abstract] [Full Text] [Related]

  • 39. Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32.
    Hayashida S, Yamasaki K, Asada Y, Soeda E, Niikawa N, Kishino T.
    Genomics; 2000 Jun 01; 66(2):221-5. PubMed ID: 10860668
    [Abstract] [Full Text] [Related]

  • 40. 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
    [Abstract] [Full Text] [Related]

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