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 *

70 related articles for article (PubMed ID: 3493870)

  • 21. [Congenital dyschromatopsia. I. Genetic aspects].
    Klein D
    J Genet Hum; 1986 Jan; 34(1):75-86. PubMed ID: 3485700
    [No Abstract]   [Full Text] [Related]  

  • 22. [Genetics of congenital color vision defects. II. Rare types of color blindness].
    Krawczyński MR
    Klin Oczna; 1995; 97(1-2):39-43. PubMed ID: 7637312
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The genetic heterogeneity of spinal muscular atrophy (SMA).
    Zellweger H
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):82-9. PubMed ID: 5173130
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Frontometaphyseal dysplasia--evidence for X-linked inheritance.
    Gorlin RJ; Winter RB
    Am J Med Genet; 1980; 5(1):81-4. PubMed ID: 7395904
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Dyschromatopsia and dental agenesis. A new syndrome with a probable genetic etiology].
    Mastagni G; Riccomini P; Mastagni M
    Minerva Stomatol; 1991 Oct; 40(10):657-64. PubMed ID: 1803223
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24.
    van der Vleuten AJ; van Ravenswaaij-Arts CM; Frijns CJ; Smits AP; Hageman G; Padberg GW; Kremer H
    Eur J Hum Genet; 1998; 6(4):376-82. PubMed ID: 9781046
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.
    De bruyn A; Raeymaekers P; Mendelbaum K; Sandkuijl LA; Raes G; Delvenne V; Hirsch D; Staner L; Mendlewicz J; Van Broeckhoven C
    Am J Med Genet; 1994 Dec; 54(4):411-9. PubMed ID: 7726217
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy.
    Echaniz-Laguna A; Rousso E; Anheim M; Cossée M; Tranchant C
    Neurology; 2005 Apr; 64(8):1458-60. PubMed ID: 15851746
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Trichromatic color vision with only two spectrally distinct photopigments.
    Neitz J; Neitz M; He JC; Shevell SK
    Nat Neurosci; 1999 Oct; 2(10):884-8. PubMed ID: 10491608
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The X chromosome and the eye. The implications of recent microbiological models for clinical ophthalmology.
    Warburg M
    Hum Hered; 1974; 24(5-6):389-414. PubMed ID: 4219211
    [No Abstract]   [Full Text] [Related]  

  • 31. [Molecular genetic examination in sex-linked color blindness].
    Ladekjaer-Mikkelsen AS; Jensen H; Rosenberg T; Jørgensen AL
    Ugeskr Laeger; 1995 Aug; 157(35):4822-5. PubMed ID: 7676520
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy].
    Boehmer AL; Brinkmann AO; Niermeijer MF; Halley DJ; Drop SL
    Ned Tijdschr Geneeskd; 2001 Dec; 145(48):2326-8. PubMed ID: 11766302
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Human chromosome mapping].
    Frézal J; Nguyen Van Cong
    Nouv Presse Med; 1979 Mar; 8(10):769-74. PubMed ID: 313554
    [No Abstract]   [Full Text] [Related]  

  • 34. A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy.
    Jansen PH; Joosten EM; Jaspar HH; Vingerhoets HM
    Ann Neurol; 1986 Oct; 20(4):538-40. PubMed ID: 3789668
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failure.
    Arbizu T; Santamaría J; Gomez JM; Quílez A; Serra JP
    J Neurol Sci; 1983 Jun; 59(3):371-82. PubMed ID: 6683750
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Familial progressive bulbar-spinal muscular atrophy.
    MAGEE KR
    Neurology; 1960 Mar; 10():295-305. PubMed ID: 14419783
    [No Abstract]   [Full Text] [Related]  

  • 37. [On the familial form of progressive spinal muscular atrophy].
    FUNK F
    Fortschr Neurol Psychiatr Grenzgeb; 1962 Jun; 30():324-30. PubMed ID: 13895917
    [No Abstract]   [Full Text] [Related]  

  • 38. [Electromyographic research in neural muscular atrophy with x-chromosomal dominant heredity].
    WORATZ G; THIEME W
    Dtsch Z Nervenheilkd; 1960; 181():292-9. PubMed ID: 13786663
    [No Abstract]   [Full Text] [Related]  

  • 39. Inbreeding in recessive diseases.
    Tchen P; Bois E; Feingold J; Feingold N; Kaplan J
    Hum Genet; 1977 Sep; 38(2):163-7. PubMed ID: 302820
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Ryukyuan muscular atrophy].
    Nakazato H; Kinoshita M; Satoyoshi E
    Rinsho Shinkeigaku; 1977 May; 17(5):353-6. PubMed ID: 560283
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.