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 *

223 related articles for article (PubMed ID: 8286320)

  • 81. [Correlation of different ocular diseases of dominant inheritance. Examination of a family with microcornea, high myopia, retinitis pigmentosa, cataract and glaucoma (author's transl)].
    Schlieter F; Schroeder U
    Klin Monbl Augenheilkd; 1974 Apr; 164(4):485-9. PubMed ID: 4843833
    [No Abstract]   [Full Text] [Related]  

  • 82. Usher's syndrome, temporal bone pathology.
    Cremers CW; Delleman WJ
    Int J Pediatr Otorhinolaryngol; 1988 Oct; 16(1):23-30. PubMed ID: 3203983
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Hereditary aspects of pigmentary retinopathy.
    Jay B
    Trans Ophthalmol Soc U K (1962); 1972; 92():173-8. PubMed ID: 4515510
    [No Abstract]   [Full Text] [Related]  

  • 84. [Localization of the gene for the adult form of polycystic kidneys on the short arm of chromosome 16].
    Breuning MH; Reeders ST; Goor N; Hogewind BL; van Es LA; Pearson PL
    Ned Tijdschr Geneeskd; 1986 Apr; 130(15):689-92. PubMed ID: 3703046
    [No Abstract]   [Full Text] [Related]  

  • 85. Usher's syndrome.
    Cherry PM
    Ann Ophthalmol; 1973 Jul; 5(7):743-52. PubMed ID: 4541499
    [No Abstract]   [Full Text] [Related]  

  • 86. [Heredity in pigmented retinopathy].
    Daghfous MT; Ayed S; Ben Nejma L
    Tunis Med; 1987 Feb; 65(2):133-5. PubMed ID: 3505123
    [No Abstract]   [Full Text] [Related]  

  • 87. [Molecular genetics of pigmentary retinopathy].
    Millán JM; Nájera C; Beneyto M
    Med Clin (Barc); 1994 Jan; 102(1):30-2. PubMed ID: 8133683
    [No Abstract]   [Full Text] [Related]  

  • 88. Autosomal recessive cerebellar hypoplasia and tapeto-retinal degeneration: a new syndrome.
    Dooley JM; LaRoche GR; Tremblay F; Riding M
    Pediatr Neurol; 1992; 8(3):232-4. PubMed ID: 1622524
    [TBL] [Abstract][Full Text] [Related]  

  • 89. [Monilethrix: exclusive involvement of body hair].
    Hamm H; Echternacht-Happle K; Happle R
    Z Hautkr; 1984 Sep; 59(17):1177-8. PubMed ID: 6485460
    [TBL] [Abstract][Full Text] [Related]  

  • 90. [Mucopolysaccharidoses].
    Blehová B; Pazoutová N; Brychnác V
    Cas Lek Cesk; 1972; 111(8):186-9. PubMed ID: 4258700
    [No Abstract]   [Full Text] [Related]  

  • 91. [Usher's syndrome (association of familial pigmented retinopathy and deafness) 2 cases in a family].
    Michel M; Cotton JB; Picaud JJ; Lamit J; Destiné F; Freycon F
    Pediatrie; 1968 Dec; 23(8):948-51. PubMed ID: 5311102
    [No Abstract]   [Full Text] [Related]  

  • 92. [Pili anulati].
    Iankova R; Savova Y; Tschudomirova K
    Dermatol Monatsschr; 1989; 175(10):658-61. PubMed ID: 2591616
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Familial Alzheimer disease: a large, multigeneration German kindred.
    Frommelt P; Schnabel R; Kühne W; Nee LE; Polinsky RJ
    Alzheimer Dis Assoc Disord; 1991; 5(1):36-43. PubMed ID: 2025423
    [TBL] [Abstract][Full Text] [Related]  

  • 94. A new dominant retinitis pigmentosa family mapping to the RP18 locus on chromosome 1q11-21.
    Inglehearn CF; Tarttelin EE; Keen TJ; Bhattacharya SS; Moore AT; Taylor R; Bird AC
    J Med Genet; 1998 Sep; 35(9):788-9. PubMed ID: 9733043
    [No Abstract]   [Full Text] [Related]  

  • 95. [Chorioretinal dystrophies].
    Matsui M
    Nihon Rinsho; 1993 Jan; 51 Suppl():997-1002. PubMed ID: 8459637
    [No Abstract]   [Full Text] [Related]  

  • 96. Population genetic studies of retinitis pigmentosa.
    Boughman JA; Conneally PM; Nance WE
    Am J Hum Genet; 1980 Mar; 32(2):223-35. PubMed ID: 7386458
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Autosomal dominant inherited ventricular tachycardia.
    Rubin DA; O'Keefe A; Kay RH; McAllister A; Mendelson DM
    Am Heart J; 1992 Apr; 123(4 Pt 1):1082-4. PubMed ID: 1549981
    [No Abstract]   [Full Text] [Related]  

  • 98. [Usher's syndrome. Description of 3 cases].
    Kapuscinski WJ; Uher M; Ogielska E
    Bull Mem Soc Fr Ophtalmol; 1969; 82():147-51. PubMed ID: 5311799
    [No Abstract]   [Full Text] [Related]  

  • 99. Namaqualand hip dysplasia: an autosomal dominant entity.
    Beighton P; Christy G; Learmonth ID
    Am J Med Genet; 1984 Sep; 19(1):161-9. PubMed ID: 6496567
    [TBL] [Abstract][Full Text] [Related]  

  • 100. [An analysis of heterozygote fitness by the genes for autosomal-dominant diseases taking into account the parameters of penetrance and expressivity].
    Bazhenova MD; Al'tshuler BA
    Genetika; 1988 Aug; 24(8):1488-95. PubMed ID: 3203888
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.