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 *

58 related articles for article (PubMed ID: 3505123)

  • 21. A genetic analysis of retinitis pigmentosa.
    Shanker J; Ramesh A
    Indian J Ophthalmol; 1993 Apr; 41(1):23-5. PubMed ID: 8225518
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A family with retinitis pigmentosa and ESRD with late presentation, hypertension and absence of polyuria or salt wasting.
    Friedlaender MM; Rubinger D; Silver J; Zlotogora J; Merin S; Popovtzer MM
    Clin Nephrol; 1986 Apr; 25(4):202-6. PubMed ID: 3698352
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Figures and fantasies: the frequencies of the different genetic forms of retinitis pigmentosa.
    Jay M
    Birth Defects Orig Artic Ser; 1982; 18(6):167-73. PubMed ID: 7171752
    [No Abstract]   [Full Text] [Related]  

  • 24. Problems in detecting etiological heterogeneity in genetic disease illustrated with retinitis pigmentosa.
    Beaty TH; Boughman JA
    Am J Med Genet; 1986 Jul; 24(3):493-504. PubMed ID: 3728568
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
    Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Ahmad Z; Riazuddin S; Hejtmancik JF
    Mol Vis; 2004 Nov; 10():884-9. PubMed ID: 15570217
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Ayuso C; Garcia-Sandoval B; Najera C; Valverde D; Carballo M; Antiñolo G
    Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Distribution of the frequency of various Mendelian modes of inheritance in families with retinopathia pigmentosa. Results of an evaluation of the RP register of the Munster University Ophthalmology Clinic].
    Gerding H; Busse H
    Ophthalmologe; 1994 Jun; 91(3):322-8. PubMed ID: 8086748
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Cochleo-vestibular manifestations in retinitis pigmentosa (Usher's syndrome)].
    Torres G; Kume M; Corvera J; Prado A
    Acta Otorinolaryngol Iber Am; 1972; 23(4):517-24. PubMed ID: 4539456
    [No Abstract]   [Full Text] [Related]  

  • 29. X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.
    Sharon D; Bruns GA; McGee TL; Sandberg MA; Berson EL; Dryja TP
    Invest Ophthalmol Vis Sci; 2000 Aug; 41(9):2712-21. PubMed ID: 10937588
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Late congenital glaucoma and pigmentary retinopathy].
    Ghenoiu R; Khader N
    Oftalmologia; 1995; 39(4):333-7. PubMed ID: 7577903
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Retinitis pigmentosa, X-linked form: two kindreds.
    Schleutermann D; Pierce E; Cantolino SJ; Naidoff M; Hussels IE
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):183-4. PubMed ID: 5173139
    [No Abstract]   [Full Text] [Related]  

  • 32. A pedigree of Y-linked retinitis pigmentosa. Investigation report of a family.
    Zhao G; Xia H; Xia Y
    Chin Med J (Engl); 1995 Aug; 108(8):631-3. PubMed ID: 7587498
    [No Abstract]   [Full Text] [Related]  

  • 33. Retinitis pigmentosa, autosomal dominant type: two kindreds.
    Schleutermann D; Pierce E; Cantolino Sj; Naidoff M
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):178-9. PubMed ID: 5173137
    [No Abstract]   [Full Text] [Related]  

  • 34. [Gene diagnosis of X linked retinitis pigmentosa by linkage analysis].
    Liu M; Wei Y; Liu L
    Zhonghua Yi Xue Za Zhi; 1999 Jan; 79(1):54-6. PubMed ID: 11601008
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Autosomal dominant transmission in retinitis pigmentosa].
    Ghenoiu R
    Oftalmologia; 1993; 37(4):339-41. PubMed ID: 8286320
    [TBL] [Abstract][Full Text] [Related]  

  • 36. X-linked retinitis pigmentosa: report of a large kindred with loss of central vision and preserved peripheral function.
    Shastry BS; Trese MT
    Am J Med Genet; 1995 Nov; 59(3):401-2. PubMed ID: 8599373
    [No Abstract]   [Full Text] [Related]  

  • 37. [Variability of the clinical picture in heterozygotes of pigmented retinopathy related to sex].
    Otradovec J; Kloucek F; Kubícková Z; Balík J
    Cesk Oftalmol; 1979 Mar; 35(2):126-31. PubMed ID: 436155
    [No Abstract]   [Full Text] [Related]  

  • 38. [Study of the pedigree of a family with pigmented degeneration of the retina].
    Sonoda Y
    Nihon Ganka Kiyo; 1967 Aug; 18(8):815-9. PubMed ID: 5626004
    [No Abstract]   [Full Text] [Related]  

  • 39. Beware recessive genes.
    Phillips CI; Newton MS
    Lancet; 1981 Aug; 2(8241):293-7. PubMed ID: 6114334
    [No Abstract]   [Full Text] [Related]  

  • 40. [Comprehensive electrophysiological study of the early stage of peripheral pigmented tapetoretinal abiotrophy].
    Katsnel'son LA; Dnestrova GI; Shcherbatova OI
    Vestn Oftalmol; 1977; (5):54-7. PubMed ID: 906208
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.