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Volumn 120 A, Issue 2, 2003, Pages 272-275

Brachyolmia and spinal stenosis

Author keywords

Familial brachyolmia; Hobaek; Spinal stenosis; Spondylodysplasia

Indexed keywords

ADULT; ARTICLE; BACKACHE; BONE DYSPLASIA; BRACHYOLMIA; CASE REPORT; FAMILIAL DISEASE; FEMALE; HUMAN; KYPHOSIS; LORDOSIS; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PLATYSPONDYLY; PRIORITY JOURNAL; SCHOOL CHILD; SCOLIOSIS; SHORT STATURE; SIBLING; VERTEBRAL CANAL STENOSIS;

EID: 0041822008     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20204     Document Type: Article
Times cited : (5)

References (9)
  • 2
    • 0021086362 scopus 로고
    • Brachyolmia Hobaek type. A clinical, radiographic, and histochemical study
    • Horton WA, Langer CO, Collins BC, Dwyer C. 1983. Brachyolmia Hobaek type. A clinical, radiographic, and histochemical study. Am J Med Genet 16:201-221.
    • (1983) Am J Med Genet , vol.16 , pp. 201-221
    • Horton, W.A.1    Langer, C.O.2    Collins, B.C.3    Dwyer, C.4
  • 4
    • 0026045782 scopus 로고
    • Brachyolmia: A skeletal dysplasia with an altered mucopolysaccharide excretion
    • Sewell AC, Wern C, Pontz BF. 1991. Brachyolmia: A skeletal dysplasia with an altered mucopolysaccharide excretion. Clin Genet 40:312-317.
    • (1991) Clin Genet , vol.40 , pp. 312-317
    • Sewell, A.C.1    Wern, C.2    Pontz, B.F.3
  • 5
    • 0024340437 scopus 로고
    • Brachyolmia: Radiographic and genetic evidence of heterogeneity
    • Shohat M, Lachman R, Gruber HE, Rimoin DL. 1989. Brachyolmia: Radiographic and genetic evidence of heterogeneity. Am J Med Genet 33:209-219.
    • (1989) Am J Med Genet , vol.33 , pp. 209-219
    • Shohat, M.1    Lachman, R.2    Gruber, H.E.3    Rimoin, D.L.4
  • 7
    • 0026788251 scopus 로고
    • Spondylar dysplasia (SD)/brachyolmia (BD), type I: Search for qualitative anomalies in glycosaminoglycans
    • Toledo SPA. 1992. Spondylar dysplasia (SD)/brachyolmia (BD), type I: Search for qualitative anomalies in glycosaminoglycans. Clin Genet 42:213-214.
    • (1992) Clin Genet , vol.42 , pp. 213-214
    • Toledo, S.P.A.1
  • 8
    • 0018234844 scopus 로고
    • Recessively inherited, late onset spondylar dysplasia and peripheral corneal opacity with anomalies in urinary mucopolysaccharides: A possible error of chondroitin-6-sulfate synthesis
    • Toledo SPA, Maurao PAS, Lamego G, Alves CAR, Dietrich CP, Assis LM, Mattar E. 1978. Recessively inherited, late onset spondylar dysplasia and peripheral corneal opacity with anomalies in urinary mucopolysaccharides: A possible error of chondroitin-6-sulfate synthesis. Am J Med Genet 2:385-395.
    • (1978) Am J Med Genet , vol.2 , pp. 385-395
    • Toledo, S.P.A.1    Maurao, P.A.S.2    Lamego, G.3    Alves, C.A.R.4    Dietrich, C.P.5    Assis, L.M.6    Mattar, E.7
  • 9
    • 0029970609 scopus 로고    scopus 로고
    • A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly
    • Verloes A, Jamblin P, Koulischer L, Bourguignon JP. 1996. A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly. Clin Genet 49:2-5.
    • (1996) Clin Genet , vol.49 , pp. 2-5
    • Verloes, A.1    Jamblin, P.2    Koulischer, L.3    Bourguignon, J.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.