BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 8982144)

  • 21. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P; Blair MA; Andermann E; Andermann F; D'Agostino D; Taylor KA; Chahine L; Pandolfo M; Bradford Y; Haines JL; Abou-Khalil B
    Neurology; 2007 Jun; 68(24):2107-12. PubMed ID: 17377072
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The potential role of the elastic fiber system in adolescent idiopathic scoliosis.
    Hadley-Miller N; Mims B; Milewicz DM
    J Bone Joint Surg Am; 1994 Aug; 76(8):1193-206. PubMed ID: 8056800
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Correlation of linkage data with phenotype in eight families with Stickler syndrome.
    Wilkin DJ; Mortier GR; Johnson CL; Jones MC; de Paepe A; Shohat M; Wildin RS; Falk RE; Cohn DH
    Am J Med Genet; 1998 Nov; 80(2):121-7. PubMed ID: 9805127
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Transplantation of reconstructed human skin on nude mice: a model system to study expression of human tenascin-X and elastic fiber components.
    Zweers MC; Schalkwijk J; van Kuppevelt TH; van Vlijmen-Willems IM; Bergers M; Lethias C; Lamme EN
    Cell Tissue Res; 2005 Feb; 319(2):279-87. PubMed ID: 15558324
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Association of estrogen receptor beta gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.
    Zhang HQ; Lu SJ; Tang MX; Chen LQ; Liu SH; Guo CF; Wang XY; Chen J; Xie L
    Spine (Phila Pa 1976); 2009 Apr; 34(8):760-4. PubMed ID: 19337134
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Marfan syndrome: exclusion of genetic linkage to the COL1A2 gene.
    Tsipouras P; Børresen AL; Bamforth S; Harper PS; Berg K
    Clin Genet; 1986 Nov; 30(5):428-32. PubMed ID: 2879657
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.
    Qiu XS; Tang NL; Yeung HY; Lee KM; Hung VW; Ng BK; Ma SL; Kwok RH; Qin L; Qiu Y; Cheng JC
    Spine (Phila Pa 1976); 2007 Jul; 32(16):1748-53. PubMed ID: 17632395
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetics of familial idiopathic scoliosis.
    Miller NH
    Clin Orthop Relat Res; 2007 Sep; 462():6-10. PubMed ID: 17603389
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The etiology of idiopathic scoliosis.
    Harrington PR
    Clin Orthop Relat Res; 1977; (126):17-25. PubMed ID: 598109
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Autosomal dominant idiopathic scoliosis?
    Bell M; Teebi AS
    Am J Med Genet; 1995 Jan; 55(1):112. PubMed ID: 7702081
    [No Abstract]   [Full Text] [Related]  

  • 32. [Genetics of idiopathic scoliosis].
    Bonaïti C; Feingold J; Briard ML; Lapeyre F; Rigault P; Guivarch J
    Helv Paediatr Acta; 1976 Oct; 31(3):229-40. PubMed ID: 977374
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2.
    Kainulainen K; Savolainen A; Palotie A; Kaitila I; Rosenbloom J; Peltonen L
    Hum Genet; 1990 Feb; 84(3):233-6. PubMed ID: 1968032
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Familial scoliosis. A clinical report.
    Robin GC; Cohen T
    J Bone Joint Surg Br; 1975 May; 57(2):146-8. PubMed ID: 1141280
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Segregation of all four major fibrillar collagen genes in the Marfan syndrome.
    Ogilvie DJ; Wordsworth BP; Priestley LM; Dalgleish R; Schmidtke J; Zoll B; Sykes BC
    Am J Hum Genet; 1987 Dec; 41(6):1071-82. PubMed ID: 3479900
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Defective type I collagen in a woman patient with juvenile idiopathic scoliosis (author's transl)].
    Fischer S; Matzen KA; Stürz H; Krieg T; Müller PK
    Z Orthop Ihre Grenzgeb; 1981 Aug; 119(4):344-50. PubMed ID: 7293342
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Recent advances in the study of candidate genes for adolescent idiopathic scoliosis.
    Fendri K; Patten S; Zaouter C; Parent S; Kaufman G; Labelle H; Edery P; Moldovan F
    Stud Health Technol Inform; 2010; 158():3-7. PubMed ID: 20543391
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Osteoporosis and familial idiopathic scoliosis: association with an abnormal alpha 2(I) collagen.
    Shapiro JR; Burn VE; Chipman SD; Velis KP; Bansal M
    Connect Tissue Res; 1989; 21(1-4):117-23; discussion 124. PubMed ID: 2605936
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Genetic study in a family affected of idiopathic scoliosis (author's transl)].
    Ballesteros S; Grove HM; Campusano C; Teuber AM; Figueroa H
    Rev Med Chil; 1977 Apr; 105(4):224-6. PubMed ID: 887868
    [No Abstract]   [Full Text] [Related]  

  • 40. Polygenic threshold model with sex dimorphism in adolescent idiopathic scoliosis: the Carter effect.
    Kruse LM; Buchan JG; Gurnett CA; Dobbs MB
    J Bone Joint Surg Am; 2012 Aug; 94(16):1485-91. PubMed ID: 22992817
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.