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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 4059909)

  • 21. Linkage studies in Duchenne and Becker muscular dystrophies.
    Walker A; Hart K; Cole C; Hodgson S; Johnson L; Dubowitz V; Bobrow M
    J Med Genet; 1986 Dec; 23(6):538-47. PubMed ID: 2879925
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.
    Lindenbaum RH; Clarke G; Patel C; Moncrieff M; Hughes JT
    J Med Genet; 1979 Oct; 16(5):389-92. PubMed ID: 513085
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Is the Duchenne muscular dystrophy gene also an X-linked retinitis pigmentosa locus?
    Phelan JK; Bok D
    Mol Genet Metab; 2000 May; 70(1):81-3. PubMed ID: 10833335
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
    Brockdorff N; Cross GS; Cavanna JS; Fisher EM; Lyon MF; Davies KE; Brown SD
    Nature; 1987 Jul 9-15; 328(6126):166-8. PubMed ID: 3600793
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular genetics of the X chromosome and X-linked diseases.
    Craig IW; Goodfellow PN
    Lab Invest; 1986 Mar; 54(3):241-53. PubMed ID: 3512907
    [No Abstract]   [Full Text] [Related]  

  • 26. On the genetic length of the short arm of the human X chromosome.
    Ropers HH; Wieacker P; Wienker TF; Davies K; Williamson R
    Hum Genet; 1983; 65(1):53-5. PubMed ID: 6315564
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locus.
    Mukai S; Dryja TP; Bruns GA; Aldridge JF; Berson EL
    Am J Ophthalmol; 1985 Aug; 100(2):225-9. PubMed ID: 4025464
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic linkage study of Duchenne muscular dystrophy and hemophilia A.
    Konagaya M; Takayanagi T; Kamiya T; Takamatsu S
    Neurology; 1982 Sep; 32(9):1046-9. PubMed ID: 7202158
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mapping of the X-linked recessive retinitis pigmentosa gene. A review.
    Musarella MA
    Ophthalmic Paediatr Genet; 1990 Jun; 11(2):77-88. PubMed ID: 1974043
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.
    Yates JR; Warner JP; Smith JA; Deymeer F; Azulay JP; Hausmanowa-Petrusewicz I; Zaremba J; Borkowska J; Affara NA; Ferguson-Smith MA
    J Med Genet; 1993 Feb; 30(2):108-11. PubMed ID: 8445613
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Linkage analysis of X linked retinitis pigmentosa in the Irish population.
    Farrar GJ; Geraghty MT; Moloney JM; McConnell DJ; Humphries P
    J Med Genet; 1988 Apr; 25(4):222-6. PubMed ID: 3163380
    [TBL] [Abstract][Full Text] [Related]  

  • 32. DNA linkage analysis of X chromosome-linked chronic granulomatous disease.
    Baehner RL; Kunkel LM; Monaco AP; Haines JL; Conneally PM; Palmer C; Heerema N; Orkin SH
    Proc Natl Acad Sci U S A; 1986 May; 83(10):3398-401. PubMed ID: 3010296
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene.
    Burmeister M; Monaco AP; Gillard EF; van Ommen GJ; Affara NA; Ferguson-Smith MA; Kunkel LM; Lehrach H
    Genomics; 1988 Apr; 2(3):189-202. PubMed ID: 3397058
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Molecular genetic diagnosis in X chromosome-linked retinitis pigmentosa].
    Hogenkamp T; Wienker TF; Majewski F; Gal A
    Klin Monbl Augenheilkd; 1987 Oct; 191(4):307-9. PubMed ID: 2891868
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular analysis of human X-linked diseases.
    Davies KE; Ball SP; Dorkins HR; Forrest SM; Kenwrick SJ; King AW; Lavenir IJ; McGlade SA; Patterson MN; Smith TJ
    Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():337-43. PubMed ID: 3472730
    [No Abstract]   [Full Text] [Related]  

  • 36. A molecular genetic linkage map of mouse chromosome 7.
    Saunders AM; Seldin MF
    Genomics; 1990 Nov; 8(3):525-35. PubMed ID: 1981054
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.
    Roncuzzi L; Fadda S; Mochi M; Prosperi L; Sangiorgi S; Santamaria R; Sbarra D; Besana D; Morandi L; Rocchi M
    Am J Hum Genet; 1985 Mar; 37(2):407-17. PubMed ID: 2984927
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular genetics of the human X chromosome.
    Davies KE
    J Med Genet; 1985 Aug; 22(4):243-9. PubMed ID: 2995673
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families.
    Bergen AA; Van den Born LI; Schuurman EJ; Pinckers AJ; Van Ommen GJ; Bleekers-Wagemakers EM; Sandkuijl LA
    Ophthalmic Genet; 1995 Jun; 16(2):63-70. PubMed ID: 7493158
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy.
    Fischbeck KH; Ritter AW; Tirschwell DL; Kunkel LM; Bertelson CJ; Monaco AP; Hejtmancik JF; Boehm C; Ionasescu V; Ionasescu R
    Lancet; 1986 Jul; 2(8498):104. PubMed ID: 2873362
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.