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Volumn 118 A, Issue 3, 2003, Pages 293-295

Spontaneous expression of FRA3P in a patient with Nager syndrome [1]

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME FRAGILE SITE; CONGENITAL MALFORMATION; CYTOGENETICS; HUMAN; HYPOPLASIA; INFANT; KARYOTYPE; LETTER; LIMB MALFORMATION; MANDIBULOFACIAL DYSOSTOSIS; NAGER ACROFACIAL DYSOSTOSIS; PRIORITY JOURNAL;

EID: 0042321148     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (10)

References (17)
  • 1
    • 0026342840 scopus 로고
    • Nager acrofacial dysostoses: Male-to-male transmission in 2 families
    • Aylsworth A, Lin A, Friedman P. 1991. Nager acrofacial dysostoses: Male-to-male transmission in 2 families. Am J Med Genet 41:83-88.
    • (1991) Am J Med Genet , vol.41 , pp. 83-88
    • Aylsworth, A.1    Lin, A.2    Friedman, P.3
  • 2
    • 0027180245 scopus 로고
    • Nager acrofacial dysostosis: Minor familial manifestations supporting dominant inheritance
    • Bonthron D, MacGregor D, Barr D. 1993. Nager acrofacial dysostosis: Minor familial manifestations supporting dominant inheritance. Clin Genet 43:127-131.
    • (1993) Clin Genet , vol.43 , pp. 127-131
    • Bonthron, D.1    MacGregor, D.2    Barr, D.3
  • 5
    • 0031829384 scopus 로고    scopus 로고
    • Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndrome
    • Dreyer SD, Zhou L, Machado MA, Horton WA, Zabel B, Winterpacht A, Lee B. 1998. Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndrome. Mamm Genome 9:458-462.
    • (1998) Mamm Genome , vol.9 , pp. 458-462
    • Dreyer, S.D.1    Zhou, L.2    Machado, M.A.3    Horton, W.A.4    Zabel, B.5    Winterpacht, A.6    Lee, B.7
  • 6
    • 0032242325 scopus 로고    scopus 로고
    • Instability at chromosomal fragile sites
    • Glover TW. 1998. Instability at chromosomal fragile sites. Recent Results Cancer Res 154:185-199.
    • (1998) Recent Results Cancer Res , vol.154 , pp. 185-199
    • Glover, T.W.1
  • 9
    • 0022868406 scopus 로고
    • Rare, polymorphic, and common fragile sites: A classification
    • Hecht F. 1985. Rare, polymorphic, and common fragile sites: A classification. Hum Genet 74:207-208.
    • (1985) Hum Genet , vol.74 , pp. 207-208
    • Hecht, F.1
  • 10
    • 0031924605 scopus 로고    scopus 로고
    • Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: Implication for the mechanism of fragile site induction
    • Le Beau MM, Rassool FV, Neilly ME, Espinosa R, Glover TW, Smith DI, McKeithan TW. 1998. Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: Implication for the mechanism of fragile site induction. Hum Mol Genet 7:755-761.
    • (1998) Hum Mol Genet , vol.7 , pp. 755-761
    • Le Beau, M.M.1    Rassool, F.V.2    Neilly, M.E.3    Espinosa, R.4    Glover, T.W.5    Smith, D.I.6    McKeithan, T.W.7
  • 11
    • 0019992001 scopus 로고
    • Methotrexate-induced increase in gap formation in human chromosome band 3p14
    • Markkanen A, Heinonen K, Knuutila S, de la Chapelle A. 1982. Methotrexate-induced increase in gap formation in human chromosome band 3p14. Hereditas 96:317-319.
    • (1982) Hereditas , vol.96 , pp. 317-319
    • Markkanen, A.1    Heinonen, K.2    Knuutila, S.3    De la Chapelle, A.4
  • 12
    • 0027452302 scopus 로고
    • Acrofacial dysostoses: Review and report of a previously undescribed condition: The autosomal or X-linked dominant catania form of acrofacial dysostoses
    • Opitz J, Mollica F, Sorge G, Milana G, Cimino G, Caltabiano M. 1993. Acrofacial dysostoses: Review and report of a previously undescribed condition: The autosomal or X-linked dominant catania form of acrofacial dysostoses. Am J Med Genet 47:660-678.
    • (1993) Am J Med Genet , vol.47 , pp. 660-678
    • Opitz, J.1    Mollica, F.2    Sorge, G.3    Milana, G.4    Cimino, G.5    Caltabiano, M.6
  • 14
    • 0033590726 scopus 로고    scopus 로고
    • Deletion of 1q in a patient with acrofacial dysostosis
    • Waggoner D, Ciske D, Dowton B, Watson M. 1999. Deletion of 1q in a patient with acrofacial dysostosis. Am J Med Genet 82:301-304.
    • (1999) Am J Med Genet , vol.82 , pp. 301-304
    • Waggoner, D.1    Ciske, D.2    Dowton, B.3    Watson, M.4
  • 15
    • 0042131384 scopus 로고
    • Nager syndrome with partial duplication of the long arm of chromosome 2
    • Wagner S, Cole J. 1979. Nager syndrome with partial duplication of the long arm of chromosome 2. Am J Hum Genet 31:116A.
    • (1979) Am J Hum Genet , vol.31
    • Wagner, S.1    Cole, J.2
  • 16
    • 0033051760 scopus 로고    scopus 로고
    • Allele-specific late replication and fragility of the most active fragile site, FRA3B
    • Wang I, Darling J, Zhang JS, Huang H, Liu W, Smith DI. 1999. Allele-specific late replication and fragility of the most active fragile site, FRA3B. Hum Mol Genet 8:431-437.
    • (1999) Hum Mol Genet , vol.8 , pp. 431-437
    • Wang, I.1    Darling, J.2    Zhang, J.S.3    Huang, H.4    Liu, W.5    Smith, D.I.6
  • 17
    • 0027176020 scopus 로고
    • Preaxial acrofacial dysostosis (Nager sindrome) associated with an inhered and apparently balanced X;9 traslocation: Prenatal and postnatal late replication studies
    • Zori R, Gray B, Benet-Williams A, Driscoll D, Williams C, Zackowski J. 1993. Preaxial acrofacial dysostosis (Nager sindrome) associated with an inhered and apparently balanced X;9 traslocation: Prenatal and postnatal late replication studies. Am J Med Genet 46:379-383.
    • (1993) Am J Med Genet , vol.46 , pp. 379-383
    • Zori, R.1    Gray, B.2    Benet-Williams, A.3    Driscoll, D.4    Williams, C.5    Zackowski, J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.