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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]
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]
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]