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 *

174 related articles for article (PubMed ID: 7816707)

  • 21. Correlative radiographic, scintigraphic, and histological evaluation of exostoses.
    Lange RH; Lange TA; Rao BK
    J Bone Joint Surg Am; 1984 Dec; 66(9):1454-9. PubMed ID: 6238969
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The genotype-phenotype correlation of hereditary multiple exostoses.
    Alvarez C; Tredwell S; De Vera M; Hayden M
    Clin Genet; 2006 Aug; 70(2):122-30. PubMed ID: 16879194
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis.
    Xiao CY; Wang J; Zhang SZ; Van Hul W; Wuyts W; Qiu WM; Wu H; Zhang G
    Br J Cancer; 2001 Jul; 85(2):176-81. PubMed ID: 11461073
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fibrochondrogenesis in male twins at 24 weeks gestation.
    Bankier A; Fortune D; Duke J; Sillence DO
    Am J Med Genet; 1991 Jan; 38(1):95-8. PubMed ID: 2012139
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.
    Raskind WH; Conrad EU; Matsushita M; Wijsman EM; Wells DE; Chapman N; Sandell LJ; Wagner M; Houck J
    Hum Mutat; 1998; 11(3):231-9. PubMed ID: 9521425
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The second family with Spahr-type metaphyseal chondrodysplasia: autosomal recessive inheritance confirmed.
    Farag TI; Teebi AS
    Clin Genet; 1990 Sep; 38(3):237-9. PubMed ID: 2225533
    [No Abstract]   [Full Text] [Related]  

  • 27. Multiple hereditary exostoses and enchondromatosis.
    Jurik AG
    Best Pract Res Clin Rheumatol; 2020 Jun; 34(3):101505. PubMed ID: 32253147
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Abnormal scarring with keloid formation after osteochondroma excision in children with multiple hereditary exostoses.
    Hosalkar H; Greenberg J; Gaugler RL; Garg S; Dormans JP
    J Pediatr Orthop; 2007; 27(3):333-7. PubMed ID: 17414021
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Unusual osteo-chondrodysplasia: hereditary deforming exostoses. Apropos of a family].
    Kchir MM; Mazigh R; Chérif O; Charrad R; Mezhoud N; Hila A; Charrad A
    Tunis Med; 1987 Apr; 65(4):255-60. PubMed ID: 3333109
    [No Abstract]   [Full Text] [Related]  

  • 30. [Hereditary multiple exostoses: report of 5 cases within 3 generations in a family].
    Zhang XF; Xu YG; Chen WX
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Jun; 9(3):258-9. PubMed ID: 17582272
    [No Abstract]   [Full Text] [Related]  

  • 31. [Bessel-Hagen disease in children. Considerations of some clinical cases].
    Trifan N; Dimitriu AG; Lupu V; Mardare D; Voinescu C; Petrea O
    Rev Med Chir Soc Med Nat Iasi; 1985; 89(2):329-31. PubMed ID: 3878987
    [No Abstract]   [Full Text] [Related]  

  • 32. New syndrome: exostoses, anetodermia, brachydactyly.
    Mollica F; Li Volti S; Guarneri B
    Am J Med Genet; 1984 Dec; 19(4):665-7. PubMed ID: 6334993
    [No Abstract]   [Full Text] [Related]  

  • 33. [4 cases of multiple chondro-osseous exostoses].
    Werblińska B; Winnicki S
    Wiad Lek; 1968 Feb; 21(4):313-8. PubMed ID: 5302195
    [No Abstract]   [Full Text] [Related]  

  • 34. The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes.
    Stickens D; Clines G; Burbee D; Ramos P; Thomas S; Hogue D; Hecht JT; Lovett M; Evans GA
    Nat Genet; 1996 Sep; 14(1):25-32. PubMed ID: 8782816
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [The trichorhinophalangeal syndrome with exostoses. Description of a case].
    Naselli A; Tarateta A; Vignolo M; Asquasciati G; Becchetti S; Sénès FM
    Minerva Pediatr; 1987 Jan; 39(1-2):25-31. PubMed ID: 3496521
    [No Abstract]   [Full Text] [Related]  

  • 36. [A combination of multiple cartilaginous exostoses and enchondromatosis of bone in a family].
    Tschernikoff Z; Ditscheva L
    Radiol Diagn (Berl); 1989; 30(1):53-6. PubMed ID: 2785276
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hereditary multiple exostoses: one center's experience and review of etiology.
    Pierz KA; Stieber JR; Kusumi K; Dormans JP
    Clin Orthop Relat Res; 2002 Aug; (401):49-59. PubMed ID: 12151882
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Acute spinal cord compression in hereditary multiple exostoses.
    Aldea S; Bonneville F; Poirier J; Chiras J; George B; Carpentier A
    Acta Neurochir (Wien); 2006 Feb; 148(2):195-8; discussion 198. PubMed ID: 16311838
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Familial multiple exostoses syndrome: a phacomatosis of bone tissue.
    Volpi N; Dotti MT; Giannini F; Cappelli B; Terrosi Vagnoli P; Federico A
    Acta Neurol (Napoli); 1986 Oct; 8(5):516-27. PubMed ID: 3492091
    [No Abstract]   [Full Text] [Related]  

  • 40. Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostoses.
    Park KJ; Shin KH; Ku JL; Cho TJ; Lee SH; Choi IH; Phillipe C; Monaco AP; Porter DE; Park JG
    J Hum Genet; 1999; 44(4):230-4. PubMed ID: 10429361
    [TBL] [Abstract][Full Text] [Related]  

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