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Volumn 46, Issue 1, 1997, Pages 152-154

Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BASEMENT MEMBRANE; BOWMAN MEMBRANE; CHROMOSOME 10Q; CONGENITAL CORNEA DYSTROPHY; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; HUMAN CELL; PRIORITY JOURNAL;

EID: 0031573381     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.5028     Document Type: Article
Times cited : (56)

References (11)
  • 1
    • 0028920471 scopus 로고
    • Linkage of posterior polymorphous corneal dystrophy to 20q11
    • 1. Heon, E., et al. (1995). Linkage of posterior polymorphous corneal dystrophy to 20q11. Hum. Mol. Genet. 4: 485-488.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 485-488
    • Heon, E.1
  • 2
    • 0031003675 scopus 로고    scopus 로고
    • Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy
    • 2. Irvine, A. D., et al. (1997). Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy. Nature Genet. 16: 184-187.
    • (1997) Nature Genet. , vol.16 , pp. 184-187
    • Irvine, A.D.1
  • 3
    • 0029050398 scopus 로고
    • Reevaluation of corneal dystrophies of Bowman's layer and the anterior stroma (Reis-Bucklers and Thiel-Behnke types): A light and electron microscopic study of eight corneas and a review of the literature
    • 3. Küchle, M., Green, R., Völcker, H., and Barraquer, J. (1995). Reevaluation of corneal dystrophies of Bowman's layer and the anterior stroma (Reis-Bucklers and Thiel-Behnke types): A light and electron microscopic study of eight corneas and a review of the literature. Cornea 14: 333-354.
    • (1995) Cornea , vol.14 , pp. 333-354
    • Küchle, M.1    Green, R.2    Völcker, H.3    Barraquer, J.4
  • 5
    • 0024474928 scopus 로고
    • Reis-Bücklers' corneal dystrophy (immunofluorescent and electron microscopic studies)
    • 5. Lohse, E., et al. (1989). Reis-Bücklers' corneal dystrophy (immunofluorescent and electron microscopic studies). Cornea 8: 200-209.
    • (1989) Cornea , vol.8 , pp. 200-209
    • Lohse, E.1
  • 7
    • 0028790963 scopus 로고
    • The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
    • 7. O'Connell, J. R., and Weeks, D. E. (1995). The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nature Genet. 11: 402-408.
    • (1995) Nature Genet. , vol.11 , pp. 402-408
    • O'Connell, J.R.1    Weeks, D.E.2
  • 8
    • 0029795076 scopus 로고
    • The gene for Schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36
    • 8. Shearman, A. M., et al. (1995). The gene for Schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36. Hum. Mol. Genet. 5: 1667-1672.
    • (1995) Hum. Mol. Genet. , vol.5 , pp. 1667-1672
    • Shearman, A.M.1
  • 10
    • 0028895206 scopus 로고
    • Linkage of congenital hereditary endothelial dystrophy to chromosome 20
    • 10. Toma, N. M., et al. (1995). Linkage of congenital hereditary endothelial dystrophy to chromosome 20. Hum. Mol. Genet. 4: 2395-2398.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2395-2398
    • Toma, N.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.