BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 2570529)

  • 21. Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation.
    Clayton JF; Wright AF; Jay M; McKeown CM; Dempster M; Jay BS; Bird AC; Bhattacharya SS
    Hum Genet; 1986 Oct; 74(2):168-71. PubMed ID: 2876947
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic counseling in X-linked retinitis pigmentosa.
    Anandakrishnan I; Musarella MA
    J Pediatr Ophthalmol Strabismus; 1989; 26(3):140-5. PubMed ID: 2566670
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.
    Coleman M; Bhattacharya S; Lindsay S; Wright A; Jay M; Litt M; Craig I; Davies K
    Am J Hum Genet; 1990 Dec; 47(6):935-40. PubMed ID: 2239970
    [TBL] [Abstract][Full Text] [Related]  

  • 25. X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.
    Friedrich U; Warburg M; Wieacker P; Wienker TF; Gal A; Ropers HH
    Hum Genet; 1985; 71(2):93-9. PubMed ID: 2995237
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Carrier detection in X-linked retinitis pigmentosa by multipoint DNA analysis. Problems due to genetic heterogeneity.
    Bergen AA; Platje EJ; Craig I; Bakker E; Bleeker-Wagemakers EM; van Ommen GJ
    Ophthalmic Paediatr Genet; 1991 Jun; 12(2):99-103. PubMed ID: 1923320
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Two different genes for X-linked retinitis pigmentosa.
    Wirth B; Denton MJ; Chen JD; Neugebauer M; Halliday FB; van Schooneveld M; Donald J; Bleeker-Wagemakers EM; Pearson PL; Gal A
    Genomics; 1988 Apr; 2(3):263-6. PubMed ID: 3397063
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30320).
    Curtis D; Blank CE
    Hum Genet; 1989 Jan; 81(2):200-2. PubMed ID: 2912892
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci.
    Ott J; Mensink EJ; Thompson A; Schot JD; Schuurman RK
    Hum Genet; 1986 Nov; 74(3):280-3. PubMed ID: 2877937
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.
    Hardcastle AJ; David-Gray ZK; Jay M; Bird AC; Bhattacharya SS
    Invest Ophthalmol Vis Sci; 1997 Dec; 38(13):2750-5. PubMed ID: 9418727
    [TBL] [Abstract][Full Text] [Related]  

  • 33. DNA analysis and recombination in X-linked retinitis pigmentosa.
    Redmond RM; Graham CA; Craig IW; Nevin NC; Archer DB
    Eye (Lond); 1990; 4 ( Pt 1)():204-9. PubMed ID: 1969814
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q.
    Millán JM; Martínez F; Vilela C; Beneyto M; Prieto F; Nájera C
    Hum Genet; 1995 Aug; 96(2):216-8. PubMed ID: 7635473
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities.
    van Dorp DB; Wright AF; Carothers AD; Bleeker-Wagemakers EM
    Hum Genet; 1992 Jan; 88(3):331-4. PubMed ID: 1733835
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Linkage analysis in a large Spanish family with X-linked retinitis pigmentosa: phenotype-genotype correlation.
    Capeans C; Blanco MJ; Lareu MV; Barros F; Piñeiro A; Sanchez-Salorio M; Carracedo A
    Clin Genet; 1998 Jul; 54(1):26-32. PubMed ID: 9727736
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.
    McWilliam P; Farrar GJ; Kenna P; Bradley DG; Humphries MM; Sharp EM; McConnell DJ; Lawler M; Sheils D; Ryan C
    Genomics; 1989 Oct; 5(3):619-22. PubMed ID: 2613244
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.
    Blanton SH; Heckenlively JR; Cottingham AW; Friedman J; Sadler LA; Wagner M; Friedman LH; Daiger SP
    Genomics; 1991 Dec; 11(4):857-69. PubMed ID: 1783394
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Carrier detection in X-linked retinitis pigmentosa.
    Gurvitz A; Leigh DA; Halliday F; Lai LY; McDonald BL
    Aust N Z J Ophthalmol; 1994 May; 22(2):111-3. PubMed ID: 7917263
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
    Hong HK; Ferrell RE; Gorin MB
    Am J Hum Genet; 1994 Dec; 55(6):1173-81. PubMed ID: 7977377
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.