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Volumn 91, Issue , 2002, Pages 86-89

Positional cloning strategies for idiopathic scoliosis

Author keywords

[No Author keywords available]

Indexed keywords

DNA SEQUENCES; GENES; NUCLEIC ACIDS;

EID: 16544365467     PISSN: 09269630     EISSN: 18798365     Source Type: Book Series    
DOI: 10.3233/978-1-60750-935-6-86     Document Type: Conference Paper
Times cited : (5)

References (13)
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    • Beals, K. K. Nosologic and genetic aspects of scoliosis. Clinical Orthopaedics 93 (1973) 23-32
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    • Beals, K.K.1
  • 2
    • 0017752594 scopus 로고
    • The etiology of idiopathic scoliosis
    • Hairington, P. R. The etiology of idiopathic scoliosis. Clinical Orthopaedics 126 ( 1 9 7 7 ) 1 7-2 5
    • (1977) Clinical Orthopaedics , vol.126 , pp. 17-25
    • Hairington, P.R.1
  • 3
    • 0007861066 scopus 로고
    • Advances in the diagnosis and management of adolescent idiopathic scoliosis
    • Weinstein, S. L. Advances in the diagnosis and management of adolescent idiopathic scoliosis Journal of Pediatric Orthopaedics 11(1991) 5 6 1-3
    • (1991) Journal of Pediatric Orthopaedics , vol.11 , pp. 561-563
    • Weinstein, L.S.1
  • 4
    • 0015786694 scopus 로고
    • Genetic survey of idiopathic Scoliosis in Boston, Massachusetts
    • Riseborough, B. J., Wynne Davies, K. A. Genetic survey of idiopathic Scoliosis in Boston, Massachusetts. Journal of Bone and Joint Surgery 5 5-A (1973) 974-982
    • (1973) Journal of Bone and Joint Surgery , vol.55 A , pp. 974-982
    • Riseborough, B.J.1    Davies, W.A.K.2
  • 5
    • 0035977135 scopus 로고    scopus 로고
    • Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes
    • Blackshaw, S., Fraioli, K. E., Furukawa, T., Cepko, C. L. Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes. Cell 107 (2001) 579-589
    • (2001) Cell , vol.107 , pp. 579-589
    • Blackshaw, S.1    Fraioli, K.E.2    Furukawa, T.3    Cepko, C.L.4
  • 6
    • 0037091012 scopus 로고    scopus 로고
    • Mutations in CD2BP-disrupt binding to RYP PEST and are responsible for PAPA syndrome an autoinflammatory disorder
    • Wise, C. A., Gillum, J. D., Seidman, C. E., Lindor, N. M., Veile, K., Bashiardes, S., Lovett. M. Mutations in CD2BP-disrupt binding to RYP PEST and are responsible for PAPA syndrome an autoinflammatory disorder. Human Molecular Genetics 11 (2002) 961-969
    • (2002) Human Molecular Genetics , vol.11 , pp. 961-969
    • Wise, C.A.1    Gillum, J.D.2    Seidman, C.E.3    Lindor, N.M.4    Veile, K.5    Bashiardes, S.6    Lovett, M.7
  • 8
    • 0028907339 scopus 로고
    • Positional cloning moves from perditional to traditional
    • Collins, F. S. Positional cloning moves from perditional to traditional. Nature Genetics 9 (1995) 347-350
    • (1995) Nature Genetics , vol.9 , pp. 347-350
    • Collins, F.S.1
  • 10
    • 0028278058 scopus 로고
    • The european polycystic kidney disease consortium. the polycystic kidney disease i gene encodes a 4kb transcript and lies within a duplicated region on chromosome 16
    • The European Polycystic Kidney Disease Consortium. The polycystic kidney disease I gene encodes a 4kb transcript and lies within a duplicated region on chromosome 16. Cell 77(1994) 881-894
    • (1994) Cell , vol.77 , pp. 881-894
  • 12
    • 0026742127 scopus 로고
    • The Lowels oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate5phosphatase
    • Attree, 0., Olivos, I. M., Okabe, I., Bailey, L. C, Nelson, D. L., Lewis, K. A., Mclnnes, K. K., Nussbaum, K. L. The Lowels oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate5phosphatase. Namre. 3 5 8 (1992) 239-42
    • (1992) Namre , vol.358 , pp. 239-242
    • Attree, O.1    Olivos, I.M.2    Okabe, I.3    Bailey, L.C.4    Nelson, D.L.5    Lewis, K.A.6    McLnnes, K.K.7    Nussbaum, L.K.8
  • 13
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    • Dc novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: Clinical significance and distribution of breakpoints
    • Warburton D. Dc novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. American Journal of Human Genetics 49 (1991) 995-1013
    • (1991) American Journal of Human Genetics , vol.49 , pp. 995-1013
    • Warburton, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.