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 *

94 related articles for article (PubMed ID: 6965660)

  • 1. Different expressions of one gene for congenital achromatopsia with amblyopia in Northern Sweden.
    Nordström S; Polland W
    Hum Hered; 1980; 30(2):122-8. PubMed ID: 6965660
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Eight cases of congenital achromatopsia with amblyopia in two pedigrees from Northern Sweden.
    Polland W; Nordström S
    Acta Ophthalmol (Copenh); 1979 Aug; 57(4):653-64. PubMed ID: 316638
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Nature of hereditary transmission of complete achromasia with amblyopia].
    Eremenko NS
    Vestn Oftalmol; 1969; 82(4):84-8. PubMed ID: 5311310
    [No Abstract]   [Full Text] [Related]  

  • 4. Achromatopsia with amblyopia. I. A clinical and electroretinographical study of 39 cases.
    Auerbach E; Merin S
    Doc Ophthalmol; 1974 Apr; 37(1):79-117. PubMed ID: 4545952
    [No Abstract]   [Full Text] [Related]  

  • 5. [Intrafamilial association of complete and incomplete congenital achromatopsia with amblyopia and atypical (without amblyopia) of dominant autosomal transmission].
    Ponte F; Scialfa A
    Ann Ottalmol Clin Ocul; 1968 Jun; 94(6):608-32. PubMed ID: 5312373
    [No Abstract]   [Full Text] [Related]  

  • 6. [Complete congenital achromatopsia and incomplete achromatopsia with amblyopia].
    Trzcińska-Dabrowska Z; Kossowicz H; Szmigielski M
    Klin Oczna; 1970; 40(3):391-7. PubMed ID: 5311182
    [No Abstract]   [Full Text] [Related]  

  • 7. Total achromatopsia in two brothers.
    Madsen PH
    Acta Ophthalmol (Copenh); 1967; 45(4):587-93. PubMed ID: 5298971
    [No Abstract]   [Full Text] [Related]  

  • 8. Congenital achromatopsia in a Finnish family.
    Mäntyjärvi M
    Acta Ophthalmol (Copenh); 1978 Oct; 56(5):682-8. PubMed ID: 308762
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Achromatopsia with amblyopia. II. A psychophysical study of 5 cases.
    Auerbach E; Kripke B
    Doc Ophthalmol; 1974 Apr; 37(1):119-44. PubMed ID: 4545906
    [No Abstract]   [Full Text] [Related]  

  • 10. [A novel mutation in the CNGA3 gene responsible for incomplete achromatopsia].
    Burgueño-Montañés C; Colunga Cueva M; Costales Álvarez C
    Arch Soc Esp Oftalmol; 2014 Mar; 89(3):107-9. PubMed ID: 24269407
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [SD-OCT contribution in congenital achromatopsia diagnosis (6 patients)].
    Largueche L; Chebil A; Bouladi M; Bouraoui R; Kort F; Charfi H; El Matri L
    J Fr Ophtalmol; 2014 Apr; 37(4):296-302. PubMed ID: 24655792
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.
    Ouechtati F; Merdassi A; Bouyacoub Y; Largueche L; Derouiche K; Ouragini H; Nouira S; Tiab L; Baklouti K; Rebai A; Schorderet DF; Munier FL; Zografos L; Abdelhak S; El Matri L
    J Hum Genet; 2011 Jan; 56(1):22-8. PubMed ID: 21107338
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia.
    Kuniyoshi K; Muraki-Oda S; Ueyama H; Toyoda F; Sakuramoto H; Ogita H; Irifune M; Yamamoto S; Nakao A; Tsunoda K; Iwata T; Ohji M; Shimomura Y
    Jpn J Ophthalmol; 2016 May; 60(3):187-97. PubMed ID: 27040408
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Congenital achromatopsia and congestive cardiomyopathy].
    Puech B; Guilbert F; Dupuis C; Breviere GM
    Bull Soc Ophtalmol Fr; 1982 Feb; 82(2):265-7. PubMed ID: 6980724
    [No Abstract]   [Full Text] [Related]  

  • 15. Pingelap and Mokil Atolls: achromatopsia.
    Hussels IE; Morton NE
    Am J Hum Genet; 1972 May; 24(3):304-9. PubMed ID: 4555088
    [No Abstract]   [Full Text] [Related]  

  • 16. Incomplete achromatopsia: diagnosis in infancy.
    Keith CG
    Birth Defects Orig Artic Ser; 1982; 18(6):269-80. PubMed ID: 6983369
    [No Abstract]   [Full Text] [Related]  

  • 17. Complete achromatopsia associated with skeletal anomalies: a new autosomal recessive syndrome.
    García-Ortiz JE; García-Cruz D; Mendoza-Topete R; Quiroz-Mercado H; García-Cruz MO; Sánchez-Corona J
    Genet Couns; 2004; 15(4):455-61. PubMed ID: 15658622
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
    Nishiguchi KM; Sandberg MA; Gorji N; Berson EL; Dryja TP
    Hum Mutat; 2005 Mar; 25(3):248-58. PubMed ID: 15712225
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
    Kohl S; Varsanyi B; Antunes GA; Baumann B; Hoyng CB; Jägle H; Rosenberg T; Kellner U; Lorenz B; Salati R; Jurklies B; Farkas A; Andreasson S; Weleber RG; Jacobson SG; Rudolph G; Castellan C; Dollfus H; Legius E; Anastasi M; Bitoun P; Lev D; Sieving PA; Munier FL; Zrenner E; Sharpe LT; Cremers FP; Wissinger B
    Eur J Hum Genet; 2005 Mar; 13(3):302-8. PubMed ID: 15657609
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and genetic features of Hungarian achromatopsia patients.
    Varsányi B; Wissinger B; Kohl S; Koeppen K; Farkas A
    Mol Vis; 2005 Nov; 11():996-1001. PubMed ID: 16319819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.