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Volumn 15, Issue 2, 1996, Pages 163-165

Infantile spasms associated with proximal duplication of chromosome 15q

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN;

EID: 0030249145     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/0887-8994(96)00119-1     Document Type: Article
Times cited : (29)

References (14)
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    • (1977) Epilepsia , vol.18 , pp. 55-62
    • Fleizsar, K.A.1    Daniel, W.L.2    Imrey, P.B.3
  • 2
    • 0028158822 scopus 로고
    • A case of 15p tetrasomy associated with infantile spasms
    • [2] Kobayashi A, Ito M, Okada M, Yoshioka K. A case of 15p tetrasomy associated with infantile spasms. No To Hattatsu 1994;26: 74-7.
    • (1994) No To Hattatsu , vol.26 , pp. 74-77
    • Kobayashi, A.1    Ito, M.2    Okada, M.3    Yoshioka, K.4
  • 4
    • 0021917574 scopus 로고
    • Forty four probands with an additional "marker" chromosome
    • [4] Buckton KE, Spowart G, Newton MS, Evans HJ. Forty four probands with an additional "marker" chromosome. Hum Genet 1985; 69:353-70.
    • (1985) Hum Genet , vol.69 , pp. 353-370
    • Buckton, K.E.1    Spowart, G.2    Newton, M.S.3    Evans, H.J.4
  • 5
    • 0021331411 scopus 로고
    • Mosaic inversion duplication of chromosome 15 without phenotypic effect: Occurrence in a father and daughter
    • [5] Knight LA, Lipson M, Mann J, Bachman R. Mosaic inversion duplication of chromosome 15 without phenotypic effect: Occurrence in a father and daughter. Am J Med Genet 1984;17:649-54.
    • (1984) Am J Med Genet , vol.17 , pp. 649-654
    • Knight, L.A.1    Lipson, M.2    Mann, J.3    Bachman, R.4
  • 6
    • 0019795382 scopus 로고
    • Prenatal detection of an accessory chromosome identified as an inversion duplication(15)
    • [6] Stetten G, Sroka-Zaczek B, Corosn VL. Prenatal detection of an accessory chromosome identified as an inversion duplication(15). Hum Genet 1981;57:357-9.
    • (1981) Hum Genet , vol.57 , pp. 357-359
    • Stetten, G.1    Sroka-Zaczek, B.2    Corosn, V.L.3
  • 7
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    • 0018967253 scopus 로고
    • An extra inic(15p)(q11) chromosome in Prader-Willi syndrome
    • [8] Fujita H, Sakamoto Y, Hamamoto Y. An extra inic(15p)(q11) chromosome in Prader-Willi syndrome. Hum Genet 1980;55:409-11.
    • (1980) Hum Genet , vol.55 , pp. 409-411
    • Fujita, H.1    Sakamoto, Y.2    Hamamoto, Y.3
  • 10
    • 0027994534 scopus 로고
    • Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients
    • [10] Cheng SD, Spinner NB, Zackai EH, Knoll J. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients. Am J Hum Genet 1994;55:753-9.
    • (1994) Am J Hum Genet , vol.55 , pp. 753-759
    • Cheng, S.D.1    Spinner, N.B.2    Zackai, E.H.3    Knoll, J.4
  • 11
    • 0028205957 scopus 로고
    • Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: Clinical implications
    • [11] Leana-Cox J, Jenkins L, Palmer CG, et al. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: Clinical implications. Am J Hum Genet 1994;54:748-56.
    • (1994) Am J Hum Genet , vol.54 , pp. 748-756
    • Leana-Cox, J.1    Jenkins, L.2    Palmer, C.G.3
  • 12
    • 0028140507 scopus 로고
    • Molecular cloning and chromosomal localization of the human alpha 7-nicotinic receptor subunit gene (CHRNA7)
    • [12] Chini B, Raimond E, Elgoyhen AB, Moralli D, Balzaretti M, Heinemann S. Molecular cloning and chromosomal localization of the human alpha 7-nicotinic receptor subunit gene (CHRNA7). Genomics 1994;19:379-81.
    • (1994) Genomics , vol.19 , pp. 379-381
    • Chini, B.1    Raimond, E.2    Elgoyhen, A.B.3    Moralli, D.4    Balzaretti, M.5    Heinemann, S.6
  • 13
    • 0027508152 scopus 로고
    • High-resolution mapping of the gamma-aminobutyric-acid receptor subunit-beta-3 and alpha-5 gene-cluster on chromosome-15q11-q13, and localization of breakpoints in 2 Angelman syndrome patients
    • [13] Sinnett D, Wagstaff J, Glatt K, Woolf E, Kirkness EJ, Lalande M. High-resolution mapping of the gamma-aminobutyric-acid receptor subunit-beta-3 and alpha-5 gene-cluster on chromosome-15q11-q13, and localization of breakpoints in 2 Angelman syndrome patients. Am J Hum Genet 1993;52:1216-29.
    • (1993) Am J Hum Genet , vol.52 , pp. 1216-1229
    • Sinnett, D.1    Wagstaff, J.2    Glatt, K.3    Woolf, E.4    Kirkness, E.J.5    Lalande, M.6
  • 14
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    • Myoclonic epilepsy and a maternally derived deletion of 15pter → q13
    • [14] Mizuguchi M, Tsukamoto K, Suzuki Y, Nakagome Y. Myoclonic epilepsy and a maternally derived deletion of 15pter → q13. Clin Genet 1994;45:44-7.
    • (1994) Clin Genet , vol.45 , pp. 44-47
    • Mizuguchi, M.1    Tsukamoto, K.2    Suzuki, Y.3    Nakagome, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.