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Volumn 103, Issue 2, 1998, Pages 189-192

Molecular cloning of the chromosomal breakpoint in the LIS1 gene of a patient with isolated lissencephaly and balanced t(8;17)

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; ARTICLE; CASE REPORT; CHROMOSOME 17P; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; COSMID; FEMALE; HUMAN; INTRON; KARYOTYPING; MOLECULAR CLONING; NORMAL HUMAN; PRIORITY JOURNAL; SOUTHERN BLOTTING;

EID: 0031714588     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050805     Document Type: Article
Times cited : (13)

References (14)
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    • (1984) Addendum. Anal Biochem , vol.137 , pp. 266-267
    • Feinberg, A.P.1    Vogelstein, B.2
  • 4
    • 0027363767 scopus 로고
    • High resolution ordering of DNA markers by multi-color fluorescent in situ hybridization of prophase chromosomes
    • Inazawa J, Ariyama T, Tokino T, Tanigami A, Nakamura Y, Abe T (1994) High resolution ordering of DNA markers by multi-color fluorescent in situ hybridization of prophase chromosomes. Cytogenet Cell Genet 65:130-135
    • (1994) Cytogenet Cell Genet , vol.65 , pp. 130-135
    • Inazawa, J.1    Ariyama, T.2    Tokino, T.3    Tanigami, A.4    Nakamura, Y.5    Abe, T.6
  • 5
    • 0026518338 scopus 로고
    • Microdeletion of chromosome 17p13 as a cause of isolated lissencephaly
    • Ledbetter SA, Kuwano A, Dobyns WB, Ledbetter DH (1992) Microdeletion of chromosome 17p13 as a cause of isolated lissencephaly. Am J Hum Genet 50:182-189
    • (1992) Am J Hum Genet , vol.50 , pp. 182-189
    • Ledbetter, S.A.1    Kuwano, A.2    Dobyns, W.B.3    Ledbetter, D.H.4
  • 6
    • 0031040866 scopus 로고    scopus 로고
    • Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome
    • Nigro CL, Chong SS, Smith ACM, Dobyns WB, Carrozzo R, Ledbetter DH (1997) Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome. Hum Mol Genet 6:157-164
    • (1997) Hum Mol Genet , vol.6 , pp. 157-164
    • Nigro, C.L.1    Chong, S.S.2    Smith, A.C.M.3    Dobyns, W.B.4    Carrozzo, R.5    Ledbetter, D.H.6
  • 7
    • 0030039598 scopus 로고    scopus 로고
    • Isolation of a testis-specific cDNA on chromosome 17q from a region adjacent to the breakpoint of t(12;17) observed in a patient with acampomelic campomelic dysplasia and sex reversal
    • Ninomiya S, Isomura M, Narahara K, Seino Y, Nakamura Y (1996) Isolation of a testis-specific cDNA on chromosome 17q from a region adjacent to the breakpoint of t(12;17) observed in a patient with acampomelic campomelic dysplasia and sex reversal. Hum Mol Genet 5:69-72
    • (1996) Hum Mol Genet , vol.5 , pp. 69-72
    • Ninomiya, S.1    Isomura, M.2    Narahara, K.3    Seino, Y.4    Nakamura, Y.5
  • 8
    • 0023989064 scopus 로고
    • Improved tools for biological sequence comparison
    • Pearson WR, Lipman DJ (1988) Improved tools for biological sequence comparison. Proc Natl Acad Sci USA 85:2444-2448
    • (1988) Proc Natl Acad Sci USA , vol.85 , pp. 2444-2448
    • Pearson, W.R.1    Lipman, D.J.2
  • 10
    • 0028967353 scopus 로고
    • One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi
    • Rudiger NS, Gregersen N, Kielland-Brandt MC (1995) One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi. Nucleic Acids Res 23:256-260
    • (1995) Nucleic Acids Res , vol.23 , pp. 256-260
    • Rudiger, N.S.1    Gregersen, N.2    Kielland-Brandt, M.C.3
  • 11
  • 13
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    • A procedure for in vitro amplification of DNA segments that lie outside the boundaries of known sequences
    • Trigrlia T, Peterson MG, Kemp DJ (1988) A procedure for in vitro amplification of DNA segments that lie outside the boundaries of known sequences. Nucleic Acids Res 16:8186
    • (1988) Nucleic Acids Res , vol.16 , pp. 8186
    • Trigrlia, T.1    Peterson, M.G.2    Kemp, D.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.