These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

125 related items for PubMed ID: 6762139

  • 1. [Technics of genetic recombination and the human chromosomal map].
    Junien C.
    Ann Genet; 1982; 25(2):71-86. PubMed ID: 6762139
    [No Abstract] [Full Text] [Related]

  • 2. DNA analysis as clinical investigation: when and how?
    Jeanpierre M, Junien C.
    Ann Genet; 1984; 27(3):134-47. PubMed ID: 6095729
    [No Abstract] [Full Text] [Related]

  • 3. Recombinant DNA technology in prenatal diagnosis.
    Gosden JR, Gosden CM.
    Oxf Rev Reprod Biol; 1985; 7():73-117. PubMed ID: 3001618
    [No Abstract] [Full Text] [Related]

  • 4. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs.
    Abeysinghe SS, Chuzhanova N, Krawczak M, Ball EV, Cooper DN.
    Hum Mutat; 2003 Sep; 22(3):229-44. PubMed ID: 12938088
    [Abstract] [Full Text] [Related]

  • 5. Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20.
    Ting CN, Burgess DL, Chamberlain JS, Keith TP, Falls K, Meisler MH.
    Genomics; 1993 Jun; 16(3):698-706. PubMed ID: 8325643
    [Abstract] [Full Text] [Related]

  • 6. 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; 16(1):56-62. PubMed ID: 8486385
    [Abstract] [Full Text] [Related]

  • 7. Identifying genes within the genome: new ways for finding the needle in a haystack.
    Hochgeschwender U, Brennan MB.
    Bioessays; 1991 Mar; 13(3):139-44. PubMed ID: 1872824
    [No Abstract] [Full Text] [Related]

  • 8. Parasexual approaches to the genetics of man.
    Ruddle FH, Creagan RP.
    Annu Rev Genet; 1975 Mar; 9():407-86. PubMed ID: 1108769
    [No Abstract] [Full Text] [Related]

  • 9. [The divergent region of kinetoplast maxi-ring DNA in Crithidia oncopelti contains 2 types of repetitive sequences].
    Gütter P, Maslov DA, Kolesnikov AA.
    Dokl Akad Nauk SSSR; 1985 Mar; 281(4):988-90. PubMed ID: 4006688
    [No Abstract] [Full Text] [Related]

  • 10. Screening for genetic diseases with molecular probes.
    Davies KA, Williamson R.
    Ann Biol Clin (Paris); 1986 Mar; 44(2):112-5. PubMed ID: 3530062
    [Abstract] [Full Text] [Related]

  • 11. A microsatellite-based multipoint index map of human chromosome 22.
    Buetow KH, Duggan D, Yang B, Ludwigsen S, Puck J, Porter J, Budarf M, Spielman R, Emanuel BS.
    Genomics; 1993 Nov; 18(2):329-39. PubMed ID: 8288236
    [Abstract] [Full Text] [Related]

  • 12. Characterization of microsatellite polymorphisms DXS691 and DXS692: genetic mapping to Xq26.2-Xq27 and Xq25-Xq26.2.
    Lasser DM, Wilhelmsen KC, Nygaard TG, Tantravahi U.
    Genomics; 1993 Jun; 16(3):785-6. PubMed ID: 8325656
    [No Abstract] [Full Text] [Related]

  • 13. The clinical applications of DNA polymorphisms.
    Thein SL, Wainscoat JS.
    Dis Markers; 1986 Oct; 4(3):203-18. PubMed ID: 2898316
    [No Abstract] [Full Text] [Related]

  • 14. Cytogenetic studies in Sparus auratus (Pisces, Perciformes): molecular organization of 5S rDNA and chromosomal mapping of 5S and 45S ribosomal genes and of telomeric repeats.
    Sola L, Rossi AR, Annesi F, Gornung E.
    Hereditas; 2003 Oct; 139(3):232-6. PubMed ID: 15061807
    [No Abstract] [Full Text] [Related]

  • 15. The mouse neurofibromatosis type 2 gene maps to chromosome 11.
    Claudio JO, Malo D, Rouleau GA.
    Genomics; 1994 May 15; 21(2):437-9. PubMed ID: 8088840
    [Abstract] [Full Text] [Related]

  • 16. Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism.
    Jones EM, Menzel S, Espinosa R, Le Beau MM, Bell GI, Takeda J.
    Genomics; 1994 Sep 15; 23(2):490-1. PubMed ID: 7835902
    [Abstract] [Full Text] [Related]

  • 17. Novel sequences conserved on the human and mouse X chromosomes.
    Laval SH, Boyd Y.
    Genomics; 1993 Mar 15; 15(3):483-91. PubMed ID: 8468042
    [Abstract] [Full Text] [Related]

  • 18. Segmental duplications: an 'expanding' role in genomic instability and disease.
    Emanuel BS, Shaikh TH.
    Nat Rev Genet; 2001 Oct 15; 2(10):791-800. PubMed ID: 11584295
    [Abstract] [Full Text] [Related]

  • 19. Construction of a genetic map telomeric to HLA-A by microsatellite analysis.
    Camaschella C, Roetto A, De Sandre G, Piperno A, Totaro A, Dianzani I, Gasparini P.
    Mol Cell Probes; 1993 Oct 15; 7(5):411-4. PubMed ID: 8264675
    [Abstract] [Full Text] [Related]

  • 20. [Genetic analysis of hereditary diseases using PFLPs of DNA base sequence].
    Miki T, Nakura J, Kumahara Y, Takai S, Tateishi H, Nishisho I, Mori T.
    Rinsho Byori; 1985 Nov 15; 33 Spec No 65():151-9. PubMed ID: 2869164
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.