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Volumn 109, Issue 2, 1999, Pages 138-140

Premature centromere division in patients with multiple endocrine neoplasia type 1

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GENE PRODUCT;

EID: 0033058880     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00156-3     Document Type: Article
Times cited : (35)

References (20)
  • 1
    • 0017823411 scopus 로고
    • Non-random centromere division: A mechanism of non-disjunction causing aneuploidy?
    • Méhes K. Non-random centromere division. a mechanism of non-disjunction causing aneuploidy? Hum Hered. 28:1978;255-260.
    • (1978) Hum Hered , vol.28 , pp. 255-260
    • Méhes, K.1
  • 2
    • 0020546228 scopus 로고
    • Sequence of centromere separation: Occurrence, possible significance, and control
    • Vig B.K. Sequence of centromere separation. occurrence, possible significance, and control Cancer Genet Cytogenet. 8:1983;249-274.
    • (1983) Cancer Genet Cytogenet , vol.8 , pp. 249-274
    • Vig, B.K.1
  • 3
    • 0022631771 scopus 로고
    • Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD)
    • Fitzgerald P.H., Archer S.A., Morris C.M. Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD). Hum Genet. 72:1986;58-62.
    • (1986) Hum Genet , vol.72 , pp. 58-62
    • Fitzgerald, P.H.1    Archer, S.A.2    Morris, C.M.3
  • 4
    • 0023933769 scopus 로고
    • Parental centromere separation sequence and aneuploidy of the offspring
    • Banjnóczky K., Méhes K. Parental centromere separation sequence and aneuploidy of the offspring. Hum Genet. 78:1988;286-288.
    • (1988) Hum Genet , vol.78 , pp. 286-288
    • Banjnóczky, K.1    Méhes, K.2
  • 5
    • 0027443083 scopus 로고
    • "premature anaphase" in a couple with recurrent miscarriages
    • Banjnóczky K., Gardó S. "Premature anaphase" in a couple with recurrent miscarriages. Hum Genet. 92:1993;388-390.
    • (1993) Hum Genet , vol.92 , pp. 388-390
    • Banjnóczky, K.1    Gardó, S.2
  • 6
    • 0028832160 scopus 로고
    • Premature centromere division: A possible manifestation of chromosome instability
    • Méhes K., Bühler E.M. Premature centromere division. a possible manifestation of chromosome instability Am J Med Genet. 56:1995;76-79.
    • (1995) Am J Med Genet , vol.56 , pp. 76-79
    • Méhes, K.1    Bühler, E.M.2
  • 7
    • 0001610224 scopus 로고
    • Multiple endocrine neoplasia type 1
    • L.J. DeGroot. Philadelphia: Saunders
    • Thakker R.V. Multiple endocrine neoplasia type 1. DeGroot L.J. Endocrinology. 1995;2815-2831 Saunders, Philadelphia.
    • (1995) Endocrinology , pp. 2815-2831
    • Thakker, R.V.1
  • 11
    • 0020531162 scopus 로고
    • Chromosomal breakage in multiple endocrine adenomatosis (types I and II)
    • Gustavson K.-H., Jansson R., Öberg K. Chromosomal breakage in multiple endocrine adenomatosis (types I and II). Clin Genet. 23:1983;143-149.
    • (1983) Clin Genet , vol.23 , pp. 143-149
    • Gustavson, K.-H.1    Jansson, R.2    Öberg, K.3
  • 14
    • 0029840847 scopus 로고    scopus 로고
    • Genetic screening in hereditary multiple endocrine neoplasia type 1: Absence of a founder effect among Japanese families
    • Sakurai A., Katai M., Itakura Y., Nakajima K., Baba K., Hashizume K. Genetic screening in hereditary multiple endocrine neoplasia type 1. absence of a founder effect among Japanese families Jpn J Cancer Res. 87:1996;985-994.
    • (1996) Jpn J Cancer Res , vol.87 , pp. 985-994
    • Sakurai, A.1    Katai, M.2    Itakura, Y.3    Nakajima, K.4    Baba, K.5    Hashizume, K.6
  • 16
    • 0027359959 scopus 로고
    • Cytogenetics of multiple endocrine neoplasia syndromes: III. Analysis of an insulinoma from a subject with MEN 1 by chromosome painting
    • Maraschio P., Pezzolo A., Brandi M.L., Cortinovis M., Dainotti E., Scappaticci S., Fraccaro M. Cytogenetics of multiple endocrine neoplasia syndromes. III. Analysis of an insulinoma from a subject with MEN 1 by chromosome painting Cancer Genet Cytogenet. 70:1993;68-70.
    • (1993) Cancer Genet Cytogenet , vol.70 , pp. 68-70
    • Maraschio, P.1    Pezzolo, A.2    Brandi, M.L.3    Cortinovis, M.4    Dainotti, E.5    Scappaticci, S.6    Fraccaro, M.7
  • 18
    • 0028802374 scopus 로고
    • Genetic abnormalities in sporadic parathyroid adenomas: Loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus
    • Thompson D.B., Samowitz W.S., Odelberg S., Davis R.K., Szabo J., Heath H. III Genetic abnormalities in sporadic parathyroid adenomas. loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus J Clin Endocrinol Metab. 80:1995;3377-3380.
    • (1995) J Clin Endocrinol Metab , vol.80 , pp. 3377-3380
    • Thompson, D.B.1    Samowitz, W.S.2    Odelberg, S.3    Davis, R.K.4    Szabo, J.5    Heath H. III6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.