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.
92 related articles for article (PubMed ID: 1969680)
41. [Genes of hereditary diseases that predispose to tumors]. Thomas G Bull Cancer; 1988; 75(9):871-8. PubMed ID: 2905179 [TBL] [Abstract][Full Text] [Related]
42. Human genome mapping and its medical perspectives. Siniscalco M Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 2():25-46. PubMed ID: 9561634 [No Abstract] [Full Text] [Related]
43. Cytogenetic approaches to mouse models of human genetic diseases. Francke U Am J Pathol; 1980 Dec; 101(3 Suppl):S41-51. PubMed ID: 7192937 [No Abstract] [Full Text] [Related]
44. [Essays on current molecular genetics for lecture courses for students of the Biology Department at Moscow State University]. Sverdlov ED Mol Gen Mikrobiol Virusol; 1995; (4):3-19. PubMed ID: 8604233 [No Abstract] [Full Text] [Related]
45. Delineation of genetic predisposition to multifactorial disease: a general approach on the threshold of feasibility. Sobell JL; Heston LL; Sommer SS Genomics; 1992 Jan; 12(1):1-6. PubMed ID: 1733846 [No Abstract] [Full Text] [Related]
46. Comparative linkage maps of the rice and maize genomes. Ahn S; Tanksley SD Proc Natl Acad Sci U S A; 1993 Sep; 90(17):7980-4. PubMed ID: 8103599 [TBL] [Abstract][Full Text] [Related]
47. Genetic linkage as a cause of clinical variation in inherited disorders. Berg K Cytogenet Cell Genet; 1978; 22(1-6):618-20. PubMed ID: 752553 [No Abstract] [Full Text] [Related]
48. Analysis of linkage with disease-marker association. Tai JJ Proc Natl Sci Counc Repub China B; 1986 Oct; 10(4):250-3. PubMed ID: 3470816 [TBL] [Abstract][Full Text] [Related]
49. Masquerading repeats: paralogous pitfalls of the human genome. Eichler EE Genome Res; 1998 Aug; 8(8):758-62. PubMed ID: 9724321 [No Abstract] [Full Text] [Related]
50. Linkage analysis of two-locus diseases under single-locus and two-locus analysis models. Vieland V; Greenberg DA; Hodge SE; Ott J Cytogenet Cell Genet; 1992; 59(2-3):145-6. PubMed ID: 1737484 [No Abstract] [Full Text] [Related]
51. Haplotyping the human T-cell receptor beta-chain gene complex by use of restriction fragment length polymorphisms. Charmley P; Chao A; Concannon P; Hood L; Gatti RA Proc Natl Acad Sci U S A; 1990 Jun; 87(12):4823-7. PubMed ID: 1972281 [TBL] [Abstract][Full Text] [Related]
52. NICHD conference. Genomic imprinting: consequences of uniparental disomy for human disease. Schinzel A Am J Med Genet; 1993 Jul; 46(6):683-4. PubMed ID: 8103289 [No Abstract] [Full Text] [Related]
53. Resolution of quantitative traits into Mendelian factors by using a complete linkage map of restriction fragment length polymorphisms. Paterson AH; Lander ES; Hewitt JD; Peterson S; Lincoln SE; Tanksley SD Nature; 1988 Oct; 335(6192):721-6. PubMed ID: 2902517 [TBL] [Abstract][Full Text] [Related]
55. Ava I RFLP at the gas-1 locus on mouse chromosome 12. Colombo MP; Baracetti P; Schneider C; Cairo G Nucleic Acids Res; 1989 Jul; 17(13):5415. PubMed ID: 2569712 [No Abstract] [Full Text] [Related]
56. Molecular genetics of human chromosome 4. Gusella JA; Gilliam TC; MacDonald ME; Cheng SV; Tanzi RE J Med Genet; 1986 Jun; 23(3):193-9. PubMed ID: 2941587 [TBL] [Abstract][Full Text] [Related]
57. Soybean genetic map of RAPD markers assigned to an existing scaffold RFLP map. Ferreira AR; Foutz KR; Keim P J Hered; 2000; 91(5):392-6. PubMed ID: 10994706 [TBL] [Abstract][Full Text] [Related]
58. From the tomato to the mouse. Marx J Science; 1990 Mar; 247(4950):1541. PubMed ID: 1969680 [No Abstract] [Full Text] [Related]
59. Polymorphic DNA markers genetically linked to disease-causing genes: a review. Humphries P Ir J Med Sci; 1986 Dec; 155(12):425-30. PubMed ID: 2880827 [No Abstract] [Full Text] [Related]
60. Molecular approaches for screening of genetic diseases. Marian AJ Chest; 1995 Jul; 108(1):255-65. PubMed ID: 7606967 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]