메뉴 건너뛰기




Volumn 9, Issue 1, 1999, Pages 44-52

Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q

Author keywords

[No Author keywords available]

Indexed keywords

CONTIG; CYTOSINE; FOLIC ACID; GUANINE;

EID: 0032970115     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (51)

References (27)
  • 1
    • 0030200869 scopus 로고    scopus 로고
    • A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3
    • Arai, Y., F. Hosoda, K. Nakayama, and M. Ohki. 1996. A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3. Genomics 35: 195-206.
    • (1996) Genomics , vol.35 , pp. 195-206
    • Arai, Y.1    Hosoda, F.2    Nakayama, K.3    Ohki, M.4
  • 2
    • 0031238583 scopus 로고    scopus 로고
    • A high resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23
    • Baysal, B.E., E.M. van Schothorst, J.E. Farr, M.R. James, P. Devilee, and C.W. Richard III. 1997. A high resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23. Genomics 44: 214-221.
    • (1997) Genomics , vol.44 , pp. 214-221
    • Baysal, B.E.1    Van Schothorst, E.M.2    Farr, J.E.3    James, M.R.4    Devilee, P.5    Richard C.W. III6
  • 3
    • 0028952956 scopus 로고
    • A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q
    • Breton-Gorius, J., R. Favier, J. Guichard, D. Cherif, R. Berger, N. Debili, W. Vainchenker, and L. Douay. 1995. A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q. Blood 85: 1805-1814.
    • (1995) Blood , vol.85 , pp. 1805-1814
    • Breton-Gorius, J.1    Favier, R.2    Guichard, J.3    Cherif, D.4    Berger, R.5    Debili, N.6    Vainchenker, W.7    Douay, L.8
  • 5
    • 0027723477 scopus 로고
    • A first generation physical map of the human genome
    • Cohen, D., I. Chumakov, and J. Weissenbach. 1993. A first generation physical map of the human genome. Nature 366: 398-400.
    • (1993) Nature , vol.366 , pp. 398-400
    • Cohen, D.1    Chumakov, I.2    Weissenbach, J.3
  • 7
    • 1842328565 scopus 로고    scopus 로고
    • 11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis
    • Döhner, H., S. Stilgenbauer, M.R. James, A. Benner, T. Weilguni, M. Bentz, K. Fischer, W. Hunstein, and P. Lichter. 1997. 11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis. Blood 89: 2516-2522.
    • (1997) Blood , vol.89 , pp. 2516-2522
    • Döhner, H.1    Stilgenbauer, S.2    James, M.R.3    Benner, A.4    Weilguni, T.5    Bentz, M.6    Fischer, K.7    Hunstein, W.8    Lichter, P.9
  • 8
    • 0020793569 scopus 로고
    • A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
    • Feinberg, A.P. and B. Vogelstein. 1983. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 132: 6-13.
    • (1983) Anal. Biochem. , vol.132 , pp. 6-13
    • Feinberg, A.P.1    Vogelstein, B.2
  • 12
    • 0028557941 scopus 로고
    • Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3
    • Jones, C., P. Slijepcevic, S. Marsh, E. Baker, W.Y. Langdon, R.I. Richards, and A. Tunnacliffe. 1994. Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3. Hum. Mol. Genet. 3: 2123-2130.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 2123-2130
    • Jones, C.1    Slijepcevic, P.2    Marsh, S.3    Baker, E.4    Langdon, W.Y.5    Richards, R.I.6    Tunnacliffe, A.7
  • 18
    • 0029745041 scopus 로고    scopus 로고
    • Jacobsen syndrome: Report of a patient with severe eye anomalies, growth hormone deficiency, hypothyroidism associated with deletion 11(q23q25) and review of 52 cases
    • Pivnick, E.K., G.V.N. Velagaleti, R.S. Wilroy, M.E. Smith, S.R. Rose, R.E. Tipton, and A.T. Tharapel. 1996. Jacobsen syndrome: Report of a patient with severe eye anomalies, growth hormone deficiency, hypothyroidism associated with deletion 11(q23q25) and review of 52 cases. J. Med. Genet. 33: 772-778.
    • (1996) J. Med. Genet. , vol.33 , pp. 772-778
    • Pivnick, E.K.1    Velagaleti, G.V.N.2    Wilroy, R.S.3    Smith, M.E.4    Rose, S.R.5    Tipton, R.E.6    Tharapel, A.T.7
  • 19
    • 0030664357 scopus 로고    scopus 로고
    • Dynamic mutation: Possible mechanisms and significance in human disease
    • Richards, R.I. and G.R. Sutherland. 1997. Dynamic mutation: Possible mechanisms and significance in human disease. Trends Biochem. Sci. 22: 432-436.
    • (1997) Trends Biochem. Sci. , vol.22 , pp. 432-436
    • Richards, R.I.1    Sutherland, G.R.2
  • 26
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
    • Verkerk, A.J.M.H., M. Pieretti, J.S. Sutcliffe, Y.-H. Fu, D.P.A. Kuhl, A. Pizzuti, O. Reiner, S. Richards, M.F. Victoria, F. Zhang et al. 1991. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65: 905-914.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.M.H.1    Pieretti, M.2    Sutcliffe, J.S.3    Fu, Y.-H.4    Kuhl, D.P.A.5    Pizzuti, A.6    Reiner, O.7    Richards, S.8    Victoria, M.F.9    Zhang, F.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.