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 *

76 related articles for article (PubMed ID: 1011765)

  • 1. [Heredity in Urov disease].
    Domaev IuA
    Klin Med (Mosk); 1976 Aug; 54(8):123-6. PubMed ID: 1011765
    [No Abstract]   [Full Text] [Related]  

  • 2. [Role of the hereditary factors in the etiology of endemic Kashin-Bek disease].
    Tikhonov VA
    Klin Med (Mosk); 1977 Sep; 55(9):142-3. PubMed ID: 926730
    [No Abstract]   [Full Text] [Related]  

  • 3. [Characteristics of a number of the links in the ecosystem of an endemic Urov disease locality in Transbaikalia].
    Butko VS; Kalabukhov EP; Andreeva TA
    Gig Sanit; 1977 Mar; (3):15-8. PubMed ID: 852706
    [No Abstract]   [Full Text] [Related]  

  • 4. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease].
    Câmpeanu E; Morariu M
    Rev Roum Neurol; 1970; 7(1):47-56. PubMed ID: 5527990
    [No Abstract]   [Full Text] [Related]  

  • 5. [Apropos of Iu. A. Domaev's article, "The Problem of the Inheritance of Urov Disease"].
    Bazilevskaia ZV
    Klin Med (Mosk); 1980 Feb; 58(2):108-9. PubMed ID: 7366151
    [No Abstract]   [Full Text] [Related]  

  • 6. [Clinico-genetic study of Kashin-Bek disease].
    Domaev IuA
    Sov Med; 1976 Nov; (11):39-43. PubMed ID: 1006392
    [No Abstract]   [Full Text] [Related]  

  • 7. [Clinical genealogical analysis of vertebrogenic myodystrophic pain syndromes].
    Shmidt IR; Zaslavskiĭ ES
    Ortop Travmatol Protez; 1980 Oct; (10):15-9. PubMed ID: 7432766
    [No Abstract]   [Full Text] [Related]  

  • 8. [Geographical distribution of Erlacher-Blount disease].
    Kuvina VN; Meshchenko VM; Plaksin IT; Filatov SV; Tatarenko SV
    Ortop Travmatol Protez; 1975 Jul; (7):69-71. PubMed ID: 1230715
    [No Abstract]   [Full Text] [Related]  

  • 9. [The probable character of heredity in familial syringomyelia].
    Sirotkin VM; Pazoni I; Gimadeeva PM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):831-6. PubMed ID: 4753594
    [No Abstract]   [Full Text] [Related]  

  • 10. [The mineral element content of the blood in healthy persons living in regions of endemic goiter and Urov (Kashin-Bek) disease].
    Gordienko VP; Abramenko SA; Radomskaia VI; Gaĭdarova SS; Kupriianova GA
    Ter Arkh; 1991; 63(10):57-9. PubMed ID: 1805422
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Heredity and mental disease. An old problem as a task of modern human genetics].
    Lange V
    Fortschr Neurol Psychiatr Grenzgeb; 1972 Oct; 40(10):534-53. PubMed ID: 4485539
    [No Abstract]   [Full Text] [Related]  

  • 12. [Strümpell-Lorrain disease and HLA typing. (A family report)].
    Blanckaert D; Gallet Y; Goudemand J; Dubois B; Morel P; Fontaine G
    Ann Pediatr (Paris); 1978 Sep; 25(7):345-7. PubMed ID: 16114345
    [No Abstract]   [Full Text] [Related]  

  • 13. [Migrain families. Genetic aspects of migraine].
    Barolin GS; Sperlich D
    Fortschr Neurol Psychiatr Grenzgeb; 1969 Oct; 37(10):521-44. PubMed ID: 5196687
    [No Abstract]   [Full Text] [Related]  

  • 14. [Etiology of the Calvé-Legg Perthes syndrome. Hematologic, genetic and histologic studies].
    Hördegen KM; Kohne E; von Lüdinghausen M
    Munch Med Wochenschr; 1971 May; 113(22):856-60. PubMed ID: 5108823
    [No Abstract]   [Full Text] [Related]  

  • 15. [Fluorine content in the hard dental tissues in the inhabitants of an endemic focus of Urov disease].
    Dymshits IaM; Frolova GI
    Stomatologiia (Mosk); 1979; 58(1):82-3. PubMed ID: 283600
    [No Abstract]   [Full Text] [Related]  

  • 16. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F
    Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Prolonged Q-T syndrome. Report of a case with dominant heredity in a deaf-mute].
    Christensen O
    Ugeskr Laeger; 1982 Feb; 144(7):472-5. PubMed ID: 7080251
    [No Abstract]   [Full Text] [Related]  

  • 18. [Tricho-rhino-phalangeal syndrome. Four family cases].
    Cottin S; Le Gall G; Lorgeas JM
    Rev Rhum Mal Osteoartic; 1980 Mar; 47(3):169-73. PubMed ID: 7384726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Primary osteochondritis of the hip. I. Etiology].
    Rev Chir Orthop Reparatrice Appar Mot; 1970; 56(7):589-93. PubMed ID: 4252463
    [No Abstract]   [Full Text] [Related]  

  • 20. Dyschondrosteosis with tibia vara--report of three cases.
    Sugiura Y; Tomita A
    Jinrui Idengaku Zasshi; 1984 Mar; 29(1):7-16. PubMed ID: 6748331
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.