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Volumn 97, Issue 6, 1996, Pages 705-709

Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting

Author keywords

[No Author keywords available]

Indexed keywords

DNA TOPOISOMERASE;

EID: 0029874862     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02346176     Document Type: Article
Times cited : (61)

References (24)
  • 1
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    • Developmental abnormalities associated with long arm deletion of chromo-some no. 6
    • Bartoshesky L, Lewis MB, Pashayan HM (1978) Developmental abnormalities associated with long arm deletion of chromo-some no. 6. Clin Genet 13:69-71
    • (1978) Clin Genet , vol.13 , pp. 69-71
    • Bartoshesky, L.1    Lewis, M.B.2    Pashayan, H.M.3
  • 5
    • 0016814696 scopus 로고
    • Mental retardation and congenital malformations associated with a ring chromosome 6
    • Fried K, Rosenblatt M, Mundel G, Krikler R (1975) Mental retardation and congenital malformations associated with a ring chromosome 6. Clin Genet 7:192-196
    • (1975) Clin Genet , vol.7 , pp. 192-196
    • Fried, K.1    Rosenblatt, M.2    Mundel, G.3    Krikler, R.4
  • 6
    • 0022486678 scopus 로고
    • Distal deletion of the long arm of chromosome 6: A specific phenotype?
    • Fryns J-P, Bettens W, Berghe H van den (1986) Distal deletion of the long arm of chromosome 6: a specific phenotype? Am J Med Genet 24:175-178
    • (1986) Am J Med Genet , vol.24 , pp. 175-178
    • Fryns, J.-P.1    Bettens, W.2    Van Den Berghe, H.3
  • 8
    • 0029005783 scopus 로고
    • Coverage of chromosome 6 by chromosome microdissection: Generation of 14 subregion-specific probes
    • Guan X-Y, Meltzer PS, Burgess AC (1995) Coverage of chromosome 6 by chromosome microdissection: generation of 14 subregion-specific probes. Hum Genet 95.637-640
    • (1995) Hum Genet , vol.95 , pp. 637-640
    • Guan, X.-Y.1    Meltzer, P.S.2    Burgess, A.C.3
  • 9
    • 0025376405 scopus 로고
    • Terminal deletion of 6q and Fryns syndrome: A microdeletion/syndrome pair?
    • Krassikoff N, Sekhon GS (1990) Terminal deletion of 6q and Fryns syndrome: a microdeletion/syndrome pair? Am J Med Genet 36:363-364
    • (1990) Am J Med Genet , vol.36 , pp. 363-364
    • Krassikoff, N.1    Sekhon, G.S.2
  • 10
    • 0017646935 scopus 로고
    • Exclusion of the HLA locus from a large portion of the long arm of chromosome 6
    • Kueppers F, Dewald G, Gordon H, Pineda A (1977) Exclusion of the HLA locus from a large portion of the long arm of chromosome 6. Hum Hered 27:242-246
    • (1977) Hum Hered , vol.27 , pp. 242-246
    • Kueppers, F.1    Dewald, G.2    Gordon, H.3    Pineda, A.4
  • 12
    • 0015854751 scopus 로고
    • Translocation with loss of chromosome material in patients and various chromosome aberrations in family members
    • Mikkelsen M, Dyggve H (1973) Translocation with loss of chromosome material in patients and various chromosome aberrations in family members. Humangenetik 18:195-202
    • (1973) Humangenetik , vol.18 , pp. 195-202
    • Mikkelsen, M.1    Dyggve, H.2
  • 13
    • 0016723791 scopus 로고
    • Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations
    • Milosevic J, Kalicanin P (1975) Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations. J Ment Defic Res 19:139-144
    • (1975) J Ment Defic Res , vol.19 , pp. 139-144
    • Milosevic, J.1    Kalicanin, P.2
  • 14
    • 0015896637 scopus 로고
    • Developmental abnormalities associated with a ring chromosome 6
    • Moore CM, Heller RH, Thomas GH (1973) Developmental abnormalities associated with a ring chromosome 6. J Med Genet 10:299-303
    • (1973) J Med Genet , vol.10 , pp. 299-303
    • Moore, C.M.1    Heller, R.H.2    Thomas, G.H.3
  • 20
    • 0027236346 scopus 로고
    • Fine mapping of the human MHC class II region within chromosome band 6p21 and evaluation of probe ordering using interphase fluorescence in situ hybridization
    • Senger G, Ragoussis J, Trowsdale J, Sheer D (1993) Fine mapping of the human MHC class II region within chromosome band 6p21 and evaluation of probe ordering using interphase fluorescence in situ hybridization. Cytogenet Cell Genet 64:49-53
    • (1993) Cytogenet Cell Genet , vol.64 , pp. 49-53
    • Senger, G.1    Ragoussis, J.2    Trowsdale, J.3    Sheer, D.4
  • 21
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    • Deletion of terminal portion of 6q: Report of a case with unusual malformations
    • Shen-Schwarz S, Hill LM, Surti U, Marchese S (1989) Deletion of terminal portion of 6q: report of a case with unusual malformations. Am J Med Genet 32:81-86
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    • Shen-Schwarz, S.1    Hill, L.M.2    Surti, U.3    Marchese, S.4
  • 22
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    • Report of two cases of distal deletion of the long arm of chromosome 6
    • Stevens CA, Fineman RM, Breg WR, Silken AB (1988) Report of two cases of distal deletion of the long arm of chromosome 6. Am J Med Genet 29:807-814
    • (1988) Am J Med Genet , vol.29 , pp. 807-814
    • Stevens, C.A.1    Fineman, R.M.2    Breg, W.R.3    Silken, A.B.4
  • 23
    • 0026736251 scopus 로고
    • Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
    • Telenius H, Carter NP, Bebb CE, Nordenskjöld M, Ponder BAJ, Tunnacliff A (1992) Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13:718-725
    • (1992) Genomics , vol.13 , pp. 718-725
    • Telenius, H.1    Carter, N.P.2    Bebb, C.E.3    Nordenskjöld, M.4    Ponder, B.A.J.5    Tunnacliff, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.