메뉴 건너뛰기




Volumn 106, Issue 2-4, 2004, Pages 165-172

Human supernumeraries: Are they B chromosomes?

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOME; AUTOSOME MOSAICISM; CENTROMERE; CHROMATIN STRUCTURE; CHROMOSOME ANALYSIS; CHROMOSOME SIZE; CHROMOSOME STRUCTURE; CHROMOSOME TRANSLOCATION; CONGENITAL MALFORMATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; FAMILIAL DISEASE; FREQUENCY ANALYSIS; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENETIC STABILITY; HETEROCHROMATIN; HUMAN; MITOSIS RATE; MOLECULAR BIOLOGY; PHENOTYPIC VARIATION; POPULATION DISTRIBUTION; POPULATION GENETICS; PRIORITY JOURNAL; REVIEW; SEX DIFFERENCE; SEX RATIO; SUPERNUMERARY CHROMOSOME;

EID: 4043073599     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000079283     Document Type: Review
Times cited : (14)

References (46)
  • 2
    • 0036783383 scopus 로고    scopus 로고
    • Neocentromeres: Role in human disease, evolution, and centromere study
    • Amor DJ, Choo KHA: Neocentromeres: role in human disease, evolution, and centromere study. Am J Hum Genet 71:695-714 (2002).
    • (2002) Am J Hum Genet , vol.71 , pp. 695-714
    • Amor, D.J.1    Choo, K.H.A.2
  • 3
    • 0028027588 scopus 로고
    • Swedish survey on extra structurally abnormal chromosomes in 39,105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization
    • Blennow E, Bui TH, Kristoffersson U, Vujic M, Annerén G, Holmberg E, Norsdenskjöld M: Swedish survey on extra structurally abnormal chromosomes in 39,105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization. Prenat Diagn 14:1019-1028 (1994).
    • (1994) Prenat Diagn , vol.14 , pp. 1019-1028
    • Blennow, E.1    Bui, T.H.2    Kristoffersson, U.3    Vujic, M.4    Annerén, G.5    Holmberg, E.6    Norsdenskjöld, M.7
  • 5
    • 0029004732 scopus 로고
    • A 10-years survey, 1980.1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samples
    • Brondum-Nielsen K, Mikkelsen M: A 10-years survey, 1980.1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samples. Prenat Diagn 15:615-619 (1995).
    • (1995) Prenat Diagn , vol.15 , pp. 615-619
    • Brondum-Nielsen, K.1    Mikkelsen, M.2
  • 7
    • 0026680297 scopus 로고
    • Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes
    • Callen DF, Eyre H, Yip MY, Freemantle J, Haan EA: Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes. Am J Med Genet 43:709-715 (1992)
    • (1992) Am J Med Genet , vol.43 , pp. 709-715
    • Callen, D.F.1    Eyre, H.2    Yip, M.Y.3    Freemantle, J.4    Haan, E.A.5
  • 8
    • 0028939755 scopus 로고
    • Molecular cytogenetic characterization of a small ring X chromosome in Turner patient and in a male patient with congenital abnormalities: Role of X chromosome inactivation
    • Callen DF, Eyre HJ, Dolman G, Garrybattersby MB, McCreanor JR, Valeba A, McGill JJ: Molecular cytogenetic characterization of a small ring X chromosome in Turner patient and in a male patient with congenital abnormalities: role of X chromosome inactivation. J Med Genet 32:113-116 (1995).
    • (1995) J Med Genet , vol.32 , pp. 113-116
    • Callen, D.F.1    Eyre, H.J.2    Dolman, G.3    Garrybattersby, M.B.4    McCreanor, J.R.5    Valeba, A.6    McGill, J.J.7
  • 9
    • 4043159740 scopus 로고    scopus 로고
    • B chromosomes
    • Gregory TR (ed): Elsevier, Amsterdam
    • Camacho JPM: B chromosomes, in Gregory TR (ed): The Evolution of the Genome (Elsevier, Amsterdam 2004).
    • (2004) The Evolution of the Genome
    • Camacho, J.P.M.1
  • 10
    • 0030616727 scopus 로고    scopus 로고
    • Population dynamics of a selfish B chromosome neutralized by the standard genome in the grasshopper Eyprepocnemis plorans
    • Camacho JPM, Shaw MW, López-León MD, Pardo MC, Cabrero J: Population dynamics of a selfish B chromosome neutralized by the standard genome in the grasshopper Eyprepocnemis plorans. Am Nat 149:1030-1050 (1997).
    • (1997) Am Nat , vol.149 , pp. 1030-1050
    • Camacho, J.P.M.1    Shaw, M.W.2    López-León, M.D.3    Pardo, M.C.4    Cabrero, J.5
  • 12
    • 0037229626 scopus 로고    scopus 로고
    • The B chromosomes of the grasshopper Eyprepocnemis plorans and the intragenomic conflict
    • Camacho JPM, Cabrero J, López-León MD, Bakkali M, Perfectti F: The B chromosomes of the grasshopper Eyprepocnemis plorans and the intragenomic conflict. Genetica 117:77-84 (2003).
    • (2003) Genetica , vol.117 , pp. 77-84
    • Camacho, J.P.M.1    Cabrero, J.2    López-León, M.D.3    Bakkali, M.4    Perfectti, F.5
  • 13
    • 0035431654 scopus 로고    scopus 로고
    • Domain organization at the centromere and neocentromere
    • Choo KH: Domain organization at the centromere and neocentromere. Dev Cell 1:165-177 (2001).
    • (2001) Dev Cell , vol.1 , pp. 165-177
    • Choo, K.H.1
  • 14
    • 0032971379 scopus 로고    scopus 로고
    • Large genomic duplication map to sites of instability in Prader Willi/Angelman syndrome chromosome region (15q11→q13)
    • Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH: Large genomic duplication map to sites of instability in Prader Willi/Angelman syndrome chromosome region (15q11→q13). Hum Mol Genet 8:1025-1037 (1999).
    • (1999) Hum Mol Genet , vol.8 , pp. 1025-1037
    • Christian, S.L.1    Fantes, J.A.2    Mewborn, S.K.3    Huang, B.4    Ledbetter, D.H.5
  • 15
    • 0031831222 scopus 로고    scopus 로고
    • Supernumerary chromosomes in filamentous fungi
    • Covert SF: Supernumerary chromosomes in filamentous fungi. Curr Genet 33:311-319 (1998).
    • (1998) Curr Genet , vol.33 , pp. 311-319
    • Covert, S.F.1
  • 16
    • 0032477707 scopus 로고    scopus 로고
    • FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15. II. Review of the literature
    • Crolla JA: FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15. II. Review of the literature. Am J Med Genet 75:367-381 (1998).
    • (1998) Am J Med Genet , vol.75 , pp. 367-381
    • Crolla, J.A.1
  • 17
    • 0032477780 scopus 로고    scopus 로고
    • FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15 and 22: I. Results of 26 new cases
    • Crolla JA, Long F, Rivera H, Dennis NR: FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15 and 22: I. Results of 26 new cases. Am J Med Genet 75:355-366 (1998).
    • (1998) Am J Med Genet , vol.75 , pp. 355-366
    • Crolla, J.A.1    Long, F.2    Rivera, H.3    Dennis, N.R.4
  • 20
    • 0030897814 scopus 로고    scopus 로고
    • Comparative genomic hybridization reveals a partial de novo trisomy 6q23→qter in an infant with congenital malformations: Delineation of the phenotype
    • Erdel M, Duba HC, Verdorfer I, Lingenhel A, Geiger R, Gutenberger KH, Ludescher E, Utermann B, Utermann G: Comparative genomic hybridization reveals a partial de novo trisomy 6q23→qter in an infant with congenital malformations: delineation of the phenotype. Hum Genet 99:596-601 (1997).
    • (1997) Hum Genet , vol.99 , pp. 596-601
    • Erdel, M.1    Duba, H.C.2    Verdorfer, I.3    Lingenhel, A.4    Geiger, R.5    Gutenberger, K.H.6    Ludescher, E.7    Utermann, B.8    Utermann, G.9
  • 21
  • 22
    • 0016173775 scopus 로고
    • Bisatellited extra small metacentric chromosomes in newborn
    • Friedrich V, Nielsen J: Bisatellited extra small metacentric chromosomes in newborn. Clin Genet 5:23-31(1974).
    • (1974) Clin Genet , vol.5 , pp. 23-31
    • Friedrich, V.1    Nielsen, J.2
  • 25
    • 0035044507 scopus 로고    scopus 로고
    • Small marker chromosome identification in metaphase and interphase using centromeric multiplex FISH
    • Henegariu O, Bray-Ward P, Artan S, Vance GH, Qumsyeh M, Ward DC: Small marker chromosome identification in metaphase and interphase using centromeric multiplex FISH. Lab Invest 81:475-481 (2001).
    • (2001) Lab Invest , vol.81 , pp. 475-481
    • Henegariu, O.1    Bray-Ward, P.2    Artan, S.3    Vance, G.H.4    Qumsyeh, M.5    Ward, D.C.6
  • 27
    • 2042437650 scopus 로고    scopus 로고
    • Initial sequencing and analysis of the human genome
    • International Human Genome Sequencing Consortium: Initial sequencing and analysis of the human genome. Nature 409:860-921 (2001).
    • (2001) Nature , vol.409 , pp. 860-921
  • 29
    • 0029199676 scopus 로고
    • Tansley Review No.85. B chromosomes in plants
    • Jones RN: Tansley Review No.85. B chromosomes in plants. New Phytol 131:411-434 (1995).
    • (1995) New Phytol , vol.131 , pp. 411-434
    • Jones, R.N.1
  • 32
    • 0033972157 scopus 로고    scopus 로고
    • Neocentromeres and alpha satellite: A proposed structural code for functional human centromere DNA
    • Kock J: Neocentromeres and alpha satellite: a proposed structural code for functional human centromere DNA. Hum Mol Genet 9:149-154 (2000).
    • (2000) Hum Mol Genet , vol.9 , pp. 149-154
    • Kock, J.1
  • 33
    • 0034846169 scopus 로고    scopus 로고
    • AcroM fluorescent in situ hybridization analyses of marker chromosomes
    • Langer S, Fauth C, Rocchi M, Murken J, Speicher MR: AcroM fluorescent in situ hybridization analyses of marker chromosomes. Hum Genet 109:152-158 (2001).
    • (2001) Hum Genet , vol.109 , pp. 152-158
    • Langer, S.1    Fauth, C.2    Rocchi, M.3    Murken, J.4    Speicher, M.R.5
  • 36
    • 0022655407 scopus 로고
    • Congenital heart disease in supernumerary der(22),t(11;22) syndrome
    • Lin AE, Bernar J, Chi A: Congenital heart disease in supernumerary der(22),t(11;22) syndrome. Clin Genet 29:269-275 (1986).
    • (1986) Clin Genet , vol.29 , pp. 269-275
    • Lin, A.E.1    Bernar, J.2    Chi, A.3
  • 37
    • 0035051713 scopus 로고    scopus 로고
    • A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: A novel class of supernumerary marker chromosome?
    • Mackie Ogilvie C, Harrison RH, Horsley SW, Hodgson SV, Kearney L: A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome? Cytogenet Cell Genet 92:69-73 (2001).
    • (2001) Cytogenet Cell Genet , vol.92 , pp. 69-73
    • Mackie Ogilvie, C.1    Harrison, R.H.2    Horsley, S.W.3    Hodgson, S.V.4    Kearney, L.5
  • 38
    • 0026602327 scopus 로고
    • Two extra inv dup (15) chromosome and male infertility: Second case
    • Manenti E: Two extra inv dup (15) chromosome and male infertility: second case. Am J Med Genet 42:402-403 (1992).
    • (1992) Am J Med Genet , vol.42 , pp. 402-403
    • Manenti, E.1
  • 39
    • 0042320536 scopus 로고    scopus 로고
    • A supernumerary chromosome 20, identified by FISH, in a male with azoospermia. Cause or coincidence?
    • McNerlan SE, Morrison PJ, McClure N, Nevin NC: A supernumerary chromosome 20, identified by FISH, in a male with azoospermia. Cause or coincidence? Am J Med Genet 117:188-190 (2003).
    • (2003) Am J Med Genet , vol.117 , pp. 188-190
    • McNerlan, S.E.1    Morrison, P.J.2    McClure, N.3    Nevin, N.C.4
  • 42
    • 0032950170 scopus 로고    scopus 로고
    • Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping
    • Ning Y, Laundon CH, Schröch E, Buchanan P, Ried T: Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping. Prenat Diagn 19:480-482 (1999).
    • (1999) Prenat Diagn , vol.19 , pp. 480-482
    • Ning, Y.1    Laundon, C.H.2    Schröch, E.3    Buchanan, P.4    Ried, T.5
  • 43
    • 0023188243 scopus 로고
    • Pallister-Killian syndrome: Cytogenetic and molecular studies
    • Peltomaki R, Knuutila S, Rivanen A, Chapelle A: Pallister-Killian syndrome: Cytogenetic and molecular studies. Clin Genet 31:399-405 (1987).
    • (1987) Clin Genet , vol.31 , pp. 399-405
    • Peltomaki, R.1    Knuutila, S.2    Rivanen, A.3    Chapelle, A.4
  • 45
    • 0000374340 scopus 로고
    • Types of supernumerary chromosomes in maize
    • Randolph L: Types of supernumerary chromosomes in maize. Anat Rec 41:102 (1928).
    • (1928) Anat Rec , vol.41 , pp. 102
    • Randolph, L.1
  • 46
    • 0026709047 scopus 로고
    • A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)
    • Rauch A, Pfeiffer RA, Trautmann U, Liehr T, Rott HD, Ulmer R: A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH). Clin Genet 42:84-90 (1992).
    • (1992) Clin Genet , vol.42 , pp. 84-90
    • Rauch, A.1    Pfeiffer, R.A.2    Trautmann, U.3    Liehr, T.4    Rott, H.D.5    Ulmer, R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.