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Volumn 54, Issue 6, 1998, Pages 512-516

Cell proliferation rate and nuclear morphometry in Roberts syndrome

Author keywords

Growth retardation; Meningocele; Nuclear morphometry; Premature centromere separation; Proliferating cell nuclear antigen; Roberts syndrome; SC phocomelia; Tetraphocomelia

Indexed keywords

CYCLINE;

EID: 0032422708     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1998.tb03772.x     Document Type: Article
Times cited : (7)

References (18)
  • 1
    • 0001031907 scopus 로고
    • A child with double cleft of lip and palate, protrusion of the intermaxillary portion of the upper jaw and imperfect development of the bones of the four extremeties
    • Roberts JB. A child with double cleft of lip and palate, protrusion of the intermaxillary portion of the upper jaw and imperfect development of the bones of the four extremeties. Ann Surg 1919: 70: 252-253.
    • (1919) Ann Surg , vol.70 , pp. 252-253
    • Roberts, J.B.1
  • 3
    • 0027429318 scopus 로고
    • Roberts syndrome: A review of 100 cases and a new rating system for severity
    • Van Den Berg DJ, Francke U. Roberts syndrome: a review of 100 cases and a new rating system for severity. Am J Med Genet 1993: 47: 1104-1123.
    • (1993) Am J Med Genet , vol.47 , pp. 1104-1123
    • Van Den Berg, D.J.1    Francke, U.2
  • 5
    • 0024318646 scopus 로고
    • Prenatal detection of Roberts-SC phocomelia syndrome: Report of two sibs with characteristic manifestations
    • Robins DB, Ladda RL, Thieme GA, Boal DK, Emanuel BS, Zackai EH. Prenatal detection of Roberts-SC phocomelia syndrome: report of two sibs with characteristic manifestations. Am J Med Genet 1989: 32: 390-394.
    • (1989) Am J Med Genet , vol.32 , pp. 390-394
    • Robins, D.B.1    Ladda, R.L.2    Thieme, G.A.3    Boal, D.K.4    Emanuel, B.S.5    Zackai, E.H.6
  • 7
    • 0002420827 scopus 로고
    • A familiar dysmorphogenetic syndrome of limb deformities, characteristic facial appearance and associated anomalies: The 'pseudothalidomide' or 'SC-syndrome'
    • Bergsma D, McKusick V, Hall J, Scott C, eds. New York: Alan R Liss, for the National Foundation - March of Dimes. BD:OAS
    • Herrmann J, Feingold M, Tuffli GA, Opitz JM. A familiar dysmorphogenetic syndrome of limb deformities, characteristic facial appearance and associated anomalies: the 'pseudothalidomide' or 'SC-syndrome'. In: Bergsma D, McKusick V, Hall J, Scott C, eds. The Clinical Delineation of Birth Defects: Part III, Limb Malformations. New York: Alan R Liss, for the National Foundation - March of Dimes. BD:OAS, 1969: 5(3): 81-89.
    • (1969) The Clinical Delineation of Birth Defects: Part III, Limb Malformations , vol.5 , Issue.3 , pp. 81-89
    • Herrmann, J.1    Feingold, M.2    Tuffli, G.A.3    Opitz, J.M.4
  • 9
    • 0022510457 scopus 로고
    • SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma
    • Parry DM, Mulvihill JJ, Tsai S, Kaiser-Kupfer M, Cowan JM. SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma. Am J Med Genet 1986: 24: 653-672.
    • (1986) Am J Med Genet , vol.24 , pp. 653-672
    • Parry, D.M.1    Mulvihill, J.J.2    Tsai, S.3    Kaiser-Kupfer, M.4    Cowan, J.M.5
  • 10
    • 0025289046 scopus 로고
    • The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome
    • Huson SM, Rodgers CS, Hall CM, Winter RM. The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome. J Med Genet 1990: 27: 371-375.
    • (1990) J Med Genet , vol.27 , pp. 371-375
    • Huson, S.M.1    Rodgers, C.S.2    Hall, C.M.3    Winter, R.M.4
  • 11
    • 0021677553 scopus 로고
    • Abnormalities in the cell-division cycle in Roberts syndrome fibroblasts: A cellular basis for the phenotypic characteristics?
    • Tomkins DJ, Sisken JE. Abnormalities in the cell-division cycle in Roberts syndrome fibroblasts: a cellular basis for the phenotypic characteristics? Am J Hum Genet 1984: 36: 1332-1340.
    • (1984) Am J Hum Genet , vol.36 , pp. 1332-1340
    • Tomkins, D.J.1    Sisken, J.E.2
  • 12
    • 0025772088 scopus 로고
    • Studies of the mitotic and centromeric abnormalities in Roberts syndrome: Implications for a defect in the mitotic mechanism
    • Jabs EW, Tuck-Muller C, Cusano R, Rattner JB. Studies of the mitotic and centromeric abnormalities in Roberts syndrome: implications for a defect in the mitotic mechanism. Chromosoma 1991: 100: 251-261.
    • (1991) Chromosoma , vol.100 , pp. 251-261
    • Jabs, E.W.1    Tuck-Muller, C.2    Cusano, R.3    Rattner, J.B.4
  • 13
    • 26444577275 scopus 로고
    • Eine seltene menschliche Missbildung und ihre Bedeutung fur die Entwicklungsgeschichte
    • Falk E. Eine seltene menschliche Missbildung und ihre Bedeutung fur die Entwicklungsgeschichte. Virchows Arch Path Anat 1908: 192: 544-564.
    • (1908) Virchows Arch Path Anat , vol.192 , pp. 544-564
    • Falk, E.1
  • 16
    • 4243296913 scopus 로고
    • Morphological evidence of disturbed chromosome separation in Roberts syndrome: A human mitotic mutant
    • Louie E, German J. Morphological evidence of disturbed chromosome separation in Roberts syndrome: a human mitotic mutant. J Cell Biol 1983: 97: 192A.
    • (1983) J Cell Biol , vol.97
    • Louie, E.1    German, J.2
  • 18
    • 0018595224 scopus 로고
    • Roberts' syndrome. I. Cytological evidence for a disturbance in chromatid pairing
    • German J. Roberts' syndrome. I. Cytological evidence for a disturbance in chromatid pairing. Clin Genet 1979: 16: 441-447.
    • (1979) Clin Genet , vol.16 , pp. 441-447
    • German, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.