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Volumn 5, Issue 3, 1997, Pages 175-177

Tetrasomy 18p caused by paternal meiotic nondisjunction

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 18; FEMALE; HUMAN; MEIOSIS; NONDISJUNCTION; PARENT; PRESCHOOL CHILD; PRIORITY JOURNAL; TETRASOMY;

EID: 0030844677     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000484755     Document Type: Article
Times cited : (21)

References (18)
  • 2
    • 0030012071 scopus 로고    scopus 로고
    • Tetrasomy 18p de novo: Identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing
    • Eggermann T, Engels H, Moskalonek B, Nöthen MM, Müller-Navia J, Schleiermacher E, Schwanitz G, Stengel-Rutkowski S: Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing. Hum Genet 1996;97: 568-572.
    • (1996) Hum Genet , vol.97 , pp. 568-572
    • Eggermann, T.1    Engels, H.2    Moskalonek, B.3    Nöthen, M.M.4    Müller-Navia, J.5    Schleiermacher, E.6    Schwanitz, G.7    Stengel-Rutkowski, S.8
  • 4
    • 0030064773 scopus 로고    scopus 로고
    • Trisomy of human chromosome 18: Molecular studies on parental origin and cell stage of nondisjunction
    • Eggermann T, Nöthen MM, Eiben B, Hofmann D, Hinkel K, Fimmers R, Schwanitz G: Trisomy of human chromosome 18: Molecular studies on parental origin and cell stage of nondisjunction. Hum Genet 1996;97:218-223.
    • (1996) Hum Genet , vol.97 , pp. 218-223
    • Eggermann, T.1    Nöthen, M.M.2    Eiben, B.3    Hofmann, D.4    Hinkel, K.5    Fimmers, R.6    Schwanitz, G.7
  • 5
    • 0028907505 scopus 로고
    • Trisomy 18: Studies on parents and cell division of origin and the effect of aberrant recombination on nondisjunction
    • Fisher JM, Harvey JF, Morton NE, Jacobs PA: Trisomy 18: Studies on parents and cell division of origin and the effect of aberrant recombination on nondisjunction. Am J Hum Genet 1995;56:669-675.
    • (1995) Am J Hum Genet , vol.56 , pp. 669-675
    • Fisher, J.M.1    Harvey, J.F.2    Morton, N.E.3    Jacobs, P.A.4
  • 6
    • 0022627760 scopus 로고
    • The heteromorphic on chromosome 18 using restriction endonuclease Alul
    • Babu A, Verma RS: The heteromorphic on chromosome 18 using restriction endonuclease Alul. Am J Hum Genet 1986;38:549-554.
    • (1986) Am J Hum Genet , vol.38 , pp. 549-554
    • Babu, A.1    Verma, R.S.2
  • 9
    • 0024432089 scopus 로고
    • Parental origin of the extra chromosome in trisomy 18
    • Kupke KG, Müller U: Parental origin of the extra chromosome in trisomy 18. Am J Hum Genet 1989;45:599-605.
    • (1989) Am J Hum Genet , vol.45 , pp. 599-605
    • Kupke, K.G.1    Müller, U.2
  • 11
    • 0028233254 scopus 로고
    • Delineation of marker chromosomes by reverse chromosome painting using only two DOP-PCR amplified microdissected chromosomes
    • Viersbach R, Schwanitz G, Nöthen MM: Delineation of marker chromosomes by reverse chromosome painting using only two DOP-PCR amplified microdissected chromosomes. Hum Genet 1994;93:663-667.
    • (1994) Hum Genet , vol.93 , pp. 663-667
    • Viersbach, R.1    Schwanitz, G.2    Nöthen, M.M.3
  • 12
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF: A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
    • (1988) Nucleic Acids Res , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 13
    • 0027161022 scopus 로고
    • Mutation of human short tandem repeats
    • Weber JL, Wong C: Mutation of human short tandem repeats. Hum Mol Genet 1993;2: 1123-1128.
    • (1993) Hum Mol Genet , vol.2 , pp. 1123-1128
    • Weber, J.L.1    Wong, C.2
  • 14
    • 0028921591 scopus 로고
    • Integration of the 1993-94 Généthon genetic linkage map for chromosome 18 with the physical map using a somatic cell hybrid mapping panel
    • Rojas K, Silverman GA, Hudson JR, Overhauser J: Integration of the 1993-94 Généthon genetic linkage map for chromosome 18 with the physical map using a somatic cell hybrid mapping panel. Genomics 1995;25:329-330.
    • (1995) Genomics , vol.25 , pp. 329-330
    • Rojas, K.1    Silverman, G.A.2    Hudson, J.R.3    Overhauser, J.4
  • 15
    • 0027447719 scopus 로고
    • Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age
    • Antonarakis SE, Avramopoulos D, Blouin JL, Talbot CC Jr, Schinzel AA: Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age. Nature Genet 1993;3:146-150.
    • (1993) Nature Genet , vol.3 , pp. 146-150
    • Antonarakis, S.E.1    Avramopoulos, D.2    Blouin, J.L.3    Talbot Jr., C.C.4    Schinzel, A.A.5
  • 17
    • 0027937004 scopus 로고
    • Nondisjunction of human acrocentric chromosomes studies of 432 trisomie fetuses and liveborns
    • Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherma S, Hassold T: Nondisjunction of human acrocentric chromosomes studies of 432 trisomie fetuses and liveborns. Hum Genet 1994;94:411-417.
    • (1994) Hum Genet , vol.94 , pp. 411-417
    • Zaragoza, M.V.1    Jacobs, P.A.2    James, R.S.3    Rogan, P.4    Sherma, S.5    Hassold, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.