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Volumn 10, Issue 12, 2002, Pages 790-800

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

(15)  Starke, Heike a   Seidel, Jörg b   Henn, Wolfram c   Reichardt, Sylvia c   Volleth, Marianne d   Stumm, Markus d   Behrend, Christine e   Sandig, Klaus R f   Kelbova, Christine g   Senger, Gabriele h   Albrecht, Beate i   Hansmann, Ingo j   Heller, Anita a   Claussen, Uwe a   Liehr, Thomas a  


Author keywords

Chromosome 9; Fish; Heteromorphism; Infertility; Multicolour banding (MCB); Satellite DNA

Indexed keywords

ACROCENTRIC CHROMOSOME; ANALYTIC METHOD; ARTICLE; CHROMOSOME 9P; CHROMOSOME 9Q; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CHROMOSOME STRUCTURE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENETIC RECOMBINATION; HETEROCHROMATIN; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR PROBE; PERICENTRIC CHROMOSOME INVERSION; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

EID: 0036930737     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200889     Document Type: Article
Times cited : (84)

References (47)
  • 1
    • 0001546238 scopus 로고    scopus 로고
    • A reply: Pericentric inversion of chromosome 9qh are 'real' but the mechanisms of their origin are highly complex
    • Verma RS. A reply: pericentric inversion of chromosome 9qh are 'real' but the mechanisms of their origin are highly complex. Hum Genet 1999; 105: 183-184.
    • (1999) Hum. Genet. , vol.105 , pp. 183-184
    • Verma, R.S.1
  • 3
    • 0003592020 scopus 로고
    • ISCN 1995: An international system for human cytogenetic nomenclature
    • Basel: S. Karger
    • Mitelman F. ISCN 1995: An international system for human cytogenetic nomenclature. Basel: S. Karger, 1995, pp 1-115.
    • (1995) , pp. 1-115
    • Mitelman, F.1
  • 4
    • 0001652137 scopus 로고    scopus 로고
    • Chromosome abnormalities and genetic counseling
    • No. 29. New York and Oxford: Oxford University Press
    • Gardner RJM, Sutherland GR: Chromosome abnormalities and genetic counseling. In: Oxford monographs on medical genetics No. 29. New York and Oxford: Oxford University Press, 1996, pp 139-158.
    • (1996) Oxford Monographs on Medical Genetics , pp. 139-158
    • Gardner, R.J.M.1    Sutherland, G.R.2
  • 5
    • 0028940010 scopus 로고
    • Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9
    • Macera MJ, Verma RS, Conte RA, Bialer MG, Klein VR: Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9. Cytogenet Cell Genet 1995; 69: 235-239.
    • (1995) Cytogenet. Cell Genet. , vol.69 , pp. 235-239
    • Macera, M.J.1    Verma, R.S.2    Conte, R.A.3    Bialer, M.G.4    Klein, V.R.5
  • 6
    • 0029873238 scopus 로고    scopus 로고
    • Breakpoints in alpha, beta, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions
    • Ramesh KH, Verma RS: Breakpoints in alpha, beta, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions. J Med Genet 1996; 33: 395-398.
    • (1996) J. Med. Genet. , vol.33 , pp. 395-398
    • Ramesh, K.H.1    Verma, R.S.2
  • 7
    • 0029853176 scopus 로고    scopus 로고
    • Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9
    • Samonte RV, Conte RA, Ramesh KH, Verma RS: Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9. Hum Genet 1996; 98: 576-580.
    • (1996) Hum. Genet. , vol.98 , pp. 576-580
    • Samonte, R.V.1    Conte, R.A.2    Ramesh, K.H.3    Verma, R.S.4
  • 8
    • 0035475786 scopus 로고    scopus 로고
    • Lessons from the human genome: Transitions between euchromatin and heterochromatin
    • Horvath JE, Bailey JA, Locke DP, Eichler EE: Lessons from the human genome: transitions between euchromatin and heterochromatin. Hum Mol Genet 2001; 10: 2215-2223.
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 2215-2223
    • Horvath, J.E.1    Bailey, J.A.2    Locke, D.P.3    Eichler, E.E.4
  • 10
    • 0001242948 scopus 로고    scopus 로고
    • Multicolor-FISH-the identification of chromosome aberrations by 24 colors
    • Senger G, Chudoba I, Plesch A: Multicolor-FISH-the identification of chromosome aberrations by 24 colors. BIOforum 1998; 9: 499-503.
    • (1998) BIOforum , vol.9 , pp. 499-503
    • Senger, G.1    Chudoba, I.2    Plesch, A.3
  • 11
    • 0034867376 scopus 로고    scopus 로고
    • Reconstruction of the female Gorilla gorilla karyotype by Zoo-FISH using 25-color FISH and multicolor banding (MCB)
    • Mrasek K, Heller A, Rubtsov N et al: Reconstruction of the female Gorilla gorilla karyotype by Zoo-FISH using 25-color FISH and multicolor banding (MCB). Cytogenet Cell Genet; 93: 242-248.
    • Cytogenet. Cell Genet. , vol.93 , pp. 242-248
    • Mrasek, K.1    Heller, A.2    Rubtsov, N.3
  • 12
    • 0000617458 scopus 로고
    • Direct preparation of uncultured EDTA-treated or heparinized blood for interphase FISH analysis
    • Liehr T, Thoma T, Kammler K et al: Direct preparation of uncultured EDTA-treated or heparinized blood for interphase FISH analysis. Appl Cytogenet 1995; 21: 185-188.
    • (1995) Appl. Cytogenet. , vol.21 , pp. 185-188
    • Liehr, T.1    Thoma, T.2    Kammler, K.3
  • 14
    • 0029912473 scopus 로고    scopus 로고
    • Karyotyping human chromosomes by combinatorial multi-fluor FISH
    • Speicher MR, Gwyn Ballard S, Ward DC: Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 1996; 12: 368-375.
    • (1996) Nat. Genet. , vol.12 , pp. 368-375
    • Speicher, M.R.1    Gwyn Ballard, S.2    Ward, D.C.3
  • 16
    • 0028843747 scopus 로고
    • Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis
    • Müller-Navia J, Nebel A, Schleiermacher E: Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis. Hum Genet 1995; 96: 661-667.
    • (1995) Hum. Genet. , vol.96 , pp. 661-667
    • Müller-Navia, J.1    Nebel, A.2    Schleiermacher, E.3
  • 17
    • 0027463306 scopus 로고
    • Genetic consequences of 'euchromatic' band within 9qh region
    • Luke S, Verma RS: Genetic consequences of 'euchromatic' band within 9qh region. Am J Med Genet 1993; 45: 107.
    • (1993) Am. J. Med. Genet. , vol.45 , pp. 107
    • Luke, S.1    Verma, R.S.2
  • 18
    • 0027267470 scopus 로고
    • Evidence of chromosome 9 origin of the euchromatic variant band within 9qh
    • Hoo JJ, Szego K, Wong P, Roland B: Evidence of chromosome 9 origin of the euchromatic variant band within 9qh. Clin Genet 1993; 43: 309-311.
    • (1993) Clin. Genet. , vol.43 , pp. 309-311
    • Hoo, J.J.1    Szego, K.2    Wong, P.3    Roland, B.4
  • 20
    • 0034133818 scopus 로고    scopus 로고
    • Patterns of genomic imbalances in human solid tumors
    • (Review)
    • Gebhart E, Liehr T: Patterns of genomic imbalances in human solid tumors (Review). Int J Onc 2000; 16: 383-399.
    • (2000) Int. J. Onc. , vol.16 , pp. 383-399
    • Gebhart, E.1    Liehr, T.2
  • 21
    • 0035374548 scopus 로고    scopus 로고
    • A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients
    • Bleichert A, Fiedler W, Claussen U et al: A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients. Int J Mol Med 2001; 7: 591-595.
    • (2001) Int. J. Mol. Med. , vol.7 , pp. 591-595
    • Bleichert, A.1    Fiedler, W.2    Claussen, U.3
  • 22
    • 85142954725 scopus 로고    scopus 로고
    • Catalogue of unbalanced chromosome aberrations in man
    • Berlin, New York: W. de Gruyter
    • Schinzel A: Catalogue of unbalanced chromosome aberrations in man. Berlin, New York: W. de Gruyter, 2001, pp. 1-966.
    • (2001) , pp. 1-966
    • Schinzel, A.1
  • 24
    • 0033934459 scopus 로고    scopus 로고
    • Acquired pericentric inversion of chromosome 9 in essential thrombocythemia
    • Wan TS, Ma SK, Chan LC: Acquired pericentric inversion of chromosome 9 in essential thrombocythemia. Hum Genet 2000; 106: 669-670.
    • (2000) Hum. Genet. , vol.106 , pp. 669-670
    • Wan, T.S.1    Ma, S.K.2    Chan, L.C.3
  • 25
    • 0028060062 scopus 로고
    • Molecular cytogenetic characterization of two types of chromosome 9 variants
    • Wang JC, Miller WA: Molecular cytogenetic characterization of two types of chromosome 9 variants. Cytogenet Cell Genet 1994; 67: 190-192.
    • (1994) Cytogenet. Cell Genet. , vol.67 , pp. 190-192
    • Wang, J.C.1    Miller, W.A.2
  • 27
    • 0029843201 scopus 로고    scopus 로고
    • Variants of chromosome 9 with additional euchromatic bands: Two case reports
    • Reddy KS: Variants of chromosome 9 with additional euchromatic bands: two case reports. Am J Med Genet 1996; 64: 536-538.
    • (1996) Am. J. Med. Genet. , vol.64 , pp. 536-538
    • Reddy, K.S.1
  • 28
    • 0027218257 scopus 로고
    • Extra G positive band on the long arm of chromosome 9
    • Knight LA, Soon GM, Tan M: Extra G positive band on the long arm of chromosome 9. J Med Genet 1993; 30: 613.
    • (1993) J. Med. Genet. , vol.30 , pp. 613
    • Knight, L.A.1    Soon, G.M.2    Tan, M.3
  • 30
    • 0017289104 scopus 로고
    • Structural variability of human chromosome 9 in relation to its evolution
    • Hansmann I: Structural variability of human chromosome 9 in relation to its evolution. Hum Genet 1976; 31: 247-262.
    • (1976) Hum. Genet. , vol.31 , pp. 247-262
    • Hansmann, I.1
  • 31
    • 0018186161 scopus 로고
    • An extra band in human 9qh+ chromosomes
    • Madan K: An extra band in human 9qh+ chromosomes. Hum Genet 1978; 43: 259-264.
    • (1978) Hum. Genet. , vol.43 , pp. 259-264
    • Madan, K.1
  • 32
    • 0018818939 scopus 로고
    • Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother
    • Berg JM, Gardner HA, Gardner RJ et al: Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother. J Med Genet 1980; 17: 144-148.
    • (1980) J. Med. Genet. , vol.17 , pp. 144-148
    • Berg, J.M.1    Gardner, H.A.2    Gardner, R.J.3
  • 33
    • 0019792123 scopus 로고
    • Structural organization of the heterochromatic region of human chromosome 9
    • Donlon TA, Magenis RE: Structural organization of the heterochromatic region of human chromosome 9. Chromosoma 1981; 84: 353-363.
    • (1981) Chromosoma , vol.84 , pp. 353-363
    • Donlon, T.A.1    Magenis, R.E.2
  • 34
    • 0020050416 scopus 로고
    • Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies
    • Silengo MC, Davi GF, Franceschini P: Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies. Hum Genet 1982; 60: 294.
    • (1982) Hum. Genet. , vol.60 , pp. 294
    • Silengo, M.C.1    Davi, G.F.2    Franceschini, P.3
  • 35
    • 0021961979 scopus 로고
    • Extra euchromatic band in the qh region of chromosome 9
    • Docherty Z, Hulten MA: Extra euchromatic band in the qh region of chromosome 9. J Med Genet 1985; 22: 156-157.
    • (1985) J. Med. Genet. , vol.22 , pp. 156-157
    • Docherty, Z.1    Hulten, M.A.2
  • 38
    • 0016159547 scopus 로고
    • Structural variation in chromosome no. 9
    • Madan K, Bobrow M: Structural variation in chromosome no. 9. Ann Génét 1974; 17: 81-86.
    • (1974) Ann. Génét , vol.17 , pp. 81-86
    • Madan, K.1    Bobrow, M.2
  • 39
    • 0027517153 scopus 로고
    • Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band
    • Verma RS, Luke S, Brennan JP, Mathews T, Conte RA, Macera MJ: Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band. Am J Hum Genet 1993; 52: 981-986.
    • (1993) Am. J. Hum. Genet. , vol.52 , pp. 981-986
    • Verma, R.S.1    Luke, S.2    Brennan, J.P.3    Mathews, T.4    Conte, R.A.5    Macera, M.J.6
  • 40
    • 0030906676 scopus 로고    scopus 로고
    • Chromosome segregation in a man heterozygous for a pericentric inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization on sperm nuclei
    • Colls P, Blanco J, Martinez-Pasarell O et al: Chromosome segregation in a man heterozygous for a pericentric inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization on sperm nuclei. Hum Genet 1997; 99: 761-765.
    • (1997) Hum. Genet. , vol.99 , pp. 761-765
    • Colls, P.1    Blanco, J.2    Martinez-Pasarell, O.3
  • 42
    • 0342470439 scopus 로고    scopus 로고
    • Chromosomal abnormalities in mentally retarded children in the Konya region-Turkey
    • Cora T, Demirel S, Acar A Chromosomal abnormalities in mentally retarded children in the Konya region-Turkey. Genet Couns 2000; 11: 53-55.
    • (2000) Genet. Couns. , vol.11 , pp. 53-55
    • Cora, T.1    Demirel, S.2    Acar, A.3
  • 43
    • 0032726797 scopus 로고    scopus 로고
    • A case of small cerebral cyst and pericentric inversion of chromosome 9 that developed schizophrenia-like psychosis
    • Miyaoka T, Seno H, Itoga M, Ishino H: A case of small cerebral cyst and pericentric inversion of chromosome 9 that developed schizophrenia-like psychosis. Psychiatry Clin Neurosci 1999; 53: 599-602.
    • (1999) Psychiatry Clin. Neurosci. , vol.53 , pp. 599-602
    • Miyaoka, T.1    Seno, H.2    Itoga, M.3    Ishino, H.4
  • 44
    • 0033885196 scopus 로고    scopus 로고
    • A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: Coincidental finding or aetiological factor?
    • Zenker M, Dorr HG: A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: coincidental finding or aetiological factor? Acta Paediatr 2000; 89: 750-751.
    • (2000) Acta Paediatr. , vol.89 , pp. 750-751
    • Zenker, M.1    Dorr, H.G.2
  • 45
    • 0034468140 scopus 로고    scopus 로고
    • Oculo-auriculovertebral (Goldenhar) spectrum associated with pericentric inversion 9: Coincidental findings or etiologic factor?
    • Stanojevic M, Stipoljev F, Koprcina B, Kurjak A: Oculo-auriculovertebral (Goldenhar) spectrum associated with pericentric inversion 9: coincidental findings or etiologic factor? J Craniofac Genet Dev Biol 2000; 20: 150-154.
    • (2000) J. Craniofac. Genet. Dev. Biol. , vol.20 , pp. 150-154
    • Stanojevic, M.1    Stipoljev, F.2    Koprcina, B.3    Kurjak, A.4
  • 46
    • 0030179193 scopus 로고    scopus 로고
    • Study of C-polymorphisms of chromosomes 1, 9 and 16 in lymphocytes of patients with laryngeal carcinoma
    • Milan C, Lamberti L: Study of C-polymorphisms of chromosomes 1, 9 and 16 in lymphocytes of patients with laryngeal carcinoma. Boll Soc Ital Biol Sper 1996; 72: 187-194.
    • (1996) Boll. Soc. Ital. Biol. Sper. , vol.72 , pp. 187-194
    • Milan, C.1    Lamberti, L.2
  • 47
    • 0032928889 scopus 로고    scopus 로고
    • Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations
    • Jackson MS, Rocchi M, Thompson G et al: Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations. Hum Mol Genet 1999; 8: 205-215.
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 205-215
    • Jackson, M.S.1    Rocchi, M.2    Thompson, G.3


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