메뉴 건너뛰기




Volumn 14, Issue 4, 1999, Pages 377-385

Chromosomal abnormalities in child psychiatric patients

Author keywords

Child psychiaty; Chromosome abnormalities

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; CHILD; DEVELOPMENTAL DISORDER; DOWN SYNDROME; FEMALE; FRAGILE X SYNDROME; GENETICS; HUMAN; KARYOTYPING; MALE; MENTAL DEFICIENCY; MENTAL DISEASE; PRESCHOOL CHILD;

EID: 0033173068     PISSN: 10118934     EISSN: None     Source Type: Journal    
DOI: 10.3346/jkms.1999.14.4.377     Document Type: Article
Times cited : (8)

References (56)
  • 1
    • 0015227656 scopus 로고
    • From gene to behavior
    • Benzer S. From gene to behavior. JAMA 1971; 18: 1015-22.
    • (1971) JAMA , vol.18 , pp. 1015-1022
    • Benzer, S.1
  • 2
    • 0015861503 scopus 로고
    • The genetics of behavior
    • Brenner S. The genetics of behavior. Br Med Bull 1973; 29: 269-71.
    • (1973) Br Med Bull , vol.29 , pp. 269-271
    • Brenner, S.1
  • 4
    • 0026783363 scopus 로고
    • Chromosomal aberrations and schizophrenia: Autosomes
    • Bassett AS. Chromosomal aberrations and schizophrenia: autosomes. Br J Psychiatry 1992; 161: 323-34.
    • (1992) Br J Psychiatry , vol.161 , pp. 323-334
    • Bassett, A.S.1
  • 6
    • 0028100408 scopus 로고
    • Psychiatric genetics: Research challenges and pathways forward
    • Rutter M. Psychiatric genetics: research challenges and pathways forward. Am J Med Genet 1994; 54: 185-98.
    • (1994) Am J Med Genet , vol.54 , pp. 185-198
    • Rutter, M.1
  • 10
    • 0025304617 scopus 로고
    • The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X
    • Sutherland GR, Baker E. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X. Clin Genet 1990; 37: 167-72.
    • (1990) Clin Genet , vol.37 , pp. 167-172
    • Sutherland, G.R.1    Baker, E.2
  • 11
    • 0016790765 scopus 로고
    • Standardization in human cytogenetics
    • Paris conference supplement. Standardization in human cytogenetics. Cytogenet Cell Genet 1975; 18: 201-38.
    • (1975) Cytogenet Cell Genet , vol.18 , pp. 201-238
  • 12
    • 84908766874 scopus 로고
    • An international system for human cytogenetic nomenclature: High resolution banding
    • 1981
    • ISCN. An international system for human cytogenetic nomenclature: high resolution banding. Birth Defects Original Article Series XVII, 1978, 1981, 1985.
    • (1978) Birth Defects Original Article Series XVII
  • 15
    • 0002418993 scopus 로고
    • The frequency of chromosomal abnormalities detected in consecutive new-born studies
    • Hook EB, Porter IH, eds. New York: Academic Press
    • Hook EB, Hamerton JL. The frequency of chromosomal abnormalities detected in consecutive new-born studies. In: Hook EB, Porter IH, eds. Population cytogenetics. New York: Academic Press, 1977: 63-79.
    • (1977) Population Cytogenetics , pp. 63-79
    • Hook, E.B.1    Hamerton, J.L.2
  • 16
    • 0025032986 scopus 로고
    • Review: The role of chromosome abnormalities in reproductive failure
    • Jacobs PA. Review: the role of chromosome abnormalities in reproductive failure. Reprod Nutr Dev Suppl 1990; 1: 63-74.
    • (1990) Reprod Nutr Dev Suppl , vol.1 , pp. 63-74
    • Jacobs, P.A.1
  • 17
    • 0024987918 scopus 로고
    • A clinical and cytogenetic study of institutionalized mental retardates
    • Kumada T. A clinical and cytogenetic study of institutionalized mental retardates. Hiroshima J Med Sci 1990; 39: 39-56.
    • (1990) Hiroshima J Med Sci , vol.39 , pp. 39-56
    • Kumada, T.1
  • 18
    • 0018934468 scopus 로고
    • Chromosome variants in children referred for cytogenetic examination from two paediatric departments during a 12-year period
    • Krag-Olsen B, Nielsen J, Dirdal M, Holm V, Haahr J, Rasmussen NH, Videbech P, Yanagisawa S. Chromosome variants in children referred for cytogenetic examination from two paediatric departments during a 12-year period. Hum Genet 1980; 56: 67-9.
    • (1980) Hum Genet , vol.56 , pp. 67-69
    • Krag-Olsen, B.1    Nielsen, J.2    Dirdal, M.3    Holm, V.4    Haahr, J.5    Rasmussen, N.H.6    Videbech, P.7    Yanagisawa, S.8
  • 19
    • 0017517247 scopus 로고
    • Cytogenetic study of individuals suspected of chromosome anomalies
    • Singh DN. Cytogenetic study of individuals suspected of chromosome anomalies. Clin Pediatr 1977; 16: 619-22.
    • (1977) Clin Pediatr , vol.16 , pp. 619-622
    • Singh, D.N.1
  • 20
    • 0018838859 scopus 로고
    • Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: A report of 357 cases
    • Verma RS, Dosik H. Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases. Clin Genet 1980; 17: 305-8.
    • (1980) Clin Genet , vol.17 , pp. 305-308
    • Verma, R.S.1    Dosik, H.2
  • 21
    • 0015258196 scopus 로고
    • Chromosome findings in 700 children referred to a psychiatric clinic
    • Crandall BF, Carrel RE, Sparkes RS. Chromosome findings in 700 children referred to a psychiatric clinic. J Pediatr 1972; 80: 62-8.
    • (1972) J Pediatr , vol.80 , pp. 62-68
    • Crandall, B.F.1    Carrel, R.E.2    Sparkes, R.S.3
  • 22
    • 0029197021 scopus 로고
    • Cytogenetic studies in clinical diagnosis - Analysis of 1611 examination results
    • Bocian E, Mazurczak T, Stanczak H. Cytogenetic studies in clinical diagnosis - analysis of 1611 examination results. Przegl Lek 1995; 52: 5-9.
    • (1995) Przegl Lek , vol.52 , pp. 5-9
    • Bocian, E.1    Mazurczak, T.2    Stanczak, H.3
  • 23
    • 0038102354 scopus 로고
    • Chromosomal abnormalities
    • Rutter M, Taylor E, Hersov L, eds. Oxford: Blackwell Scientific Publication
    • Bolton P, Holland A. Chromosomal abnormalities. In: Rutter M, Taylor E, Hersov L, eds. Child and adolescent psychiatry. 3rd ed. Oxford: Blackwell Scientific Publication, 1994: 152-71.
    • (1994) Child and Adolescent Psychiatry. 3rd Ed. , pp. 152-171
    • Bolton, P.1    Holland, A.2
  • 26
    • 0029037095 scopus 로고
    • The awareness of chromosomal disarrangements in the evaluation of child psychiatry patients
    • Levy PA, Dalton R, Shapira E. The awareness of chromosomal disarrangements in the evaluation of child psychiatry patients. Child Psychiatry Hum Dev 1995; 25: 281-7.
    • (1995) Child Psychiatry Hum Dev , vol.25 , pp. 281-287
    • Levy, P.A.1    Dalton, R.2    Shapira, E.3
  • 27
    • 0029286467 scopus 로고
    • Factors affecting age of walking by children with mental retardation
    • Kokubun M, Haishi K, Okuzumi H, Hosobuchi T. Factors affecting age of walking by children with mental retardation. Percept Mot Skills 1995; 80: 547-52.
    • (1995) Percept Mot Skills , vol.80 , pp. 547-552
    • Kokubun, M.1    Haishi, K.2    Okuzumi, H.3    Hosobuchi, T.4
  • 30
    • 0018389885 scopus 로고
    • Pericentric inversions of chromosome number 9: Benign or harmful?
    • Howard-Peebles PN, Stoddard GR. Pericentric inversions of chromosome number 9: benign or harmful? Hum Hered 1979; 29: 111-7.
    • (1979) Hum Hered , vol.29 , pp. 111-117
    • Howard-Peebles, P.N.1    Stoddard, G.R.2
  • 31
    • 0021710068 scopus 로고
    • Pericentric inversions: Problems and significance for clinical genetics
    • Kaiser P. Pericentric inversions: problems and significance for clinical genetics. Human Genet 1984; 69: 1-47.
    • (1984) Human Genet , vol.69 , pp. 1-47
    • Kaiser, P.1
  • 33
    • 0024448026 scopus 로고
    • Pericentric inversion chromosome 9 and personality disorder
    • Kumar HV. Pericentric inversion chromosome 9 and personality disorder. Br J Psychiatry 1989; 155: 408-10.
    • (1989) Br J Psychiatry , vol.155 , pp. 408-410
    • Kumar, H.V.1
  • 34
    • 0027208102 scopus 로고
    • Pericentric region of chromosome 9 is a possible candidate region for linkage study of schizophrenia
    • Nanko S, Kunugi H, Sasaki T, Fukuda R, Kawate T, Kazamatsuri H. Pericentric region of chromosome 9 is a possible candidate region for linkage study of schizophrenia. Biol Psychiatry 1993; 33: 655-8.
    • (1993) Biol Psychiatry , vol.33 , pp. 655-658
    • Nanko, S.1    Kunugi, H.2    Sasaki, T.3    Fukuda, R.4    Kawate, T.5    Kazamatsuri, H.6
  • 35
    • 0027210744 scopus 로고
    • Schizophrenia with pericentric inversion of chromosome 9: A case report
    • Nanko S. Schizophrenia with pericentric inversion of chromosome 9: a case report. Jpn J Psychiatry Neurol 1993; 47: 47-9.
    • (1993) Jpn J Psychiatry Neurol , vol.47 , pp. 47-49
    • Nanko, S.1
  • 36
    • 0018294645 scopus 로고
    • Chromosomal variants in mentally retarded and normal men
    • Soudek D, Sroka H. Chromosomal variants in mentally retarded and normal men. Clin Genet 1979; 16: 109-16.
    • (1979) Clin Genet , vol.16 , pp. 109-116
    • Soudek, D.1    Sroka, H.2
  • 37
    • 0025579568 scopus 로고
    • Pericentric inversion of chromosome 9: Prevalence in 300 Down syndrome families and molecular studies of nondisjunction
    • Serra A, Brahe C, Millington-Ward A, Neri G, Tedeschi B, Tassone F, Bova R. Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunction. Am J Med Genet Suppl 1990; 7: 162-8.
    • (1990) Am J Med Genet Suppl , vol.7 , pp. 162-168
    • Serra, A.1    Brahe, C.2    Millington-Ward, A.3    Neri, G.4    Tedeschi, B.5    Tassone, F.6    Bova, R.7
  • 38
    • 0023232927 scopus 로고
    • Chromosomal polymorphisms of 1, 9, 16 and Y in 4 major ethnic groups: A large prenatal study
    • Hsu LYF, Benn PA, Tannenbaum HL, Perils TE, Carlson AD. Chromosomal polymorphisms of 1, 9, 16 and Y in 4 major ethnic groups: a large prenatal study. Am J Med Genet 1987; 26: 95-101.
    • (1987) Am J Med Genet , vol.26 , pp. 95-101
    • Hsu, L.Y.F.1    Benn, P.A.2    Tannenbaum, H.L.3    Perils, T.E.4    Carlson, A.D.5
  • 40
    • 0027073145 scopus 로고
    • Population studies of INV (9) chromosomes in 4,300 Japanese: Incidence, sex difference and clinical significance
    • Yamada K. Population studies of INV (9) chromosomes in 4,300 Japanese: incidence, sex difference and clinical significance. Jpn J Hum Genet 1992; 37: 293-301.
    • (1992) Jpn J Hum Genet , vol.37 , pp. 293-301
    • Yamada, K.1
  • 41
    • 0029917626 scopus 로고    scopus 로고
    • Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down syndrome cytogenetic register and the association of clinical cytogeneticists
    • Mutton D, Alberman E, Hook EB. Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down syndrome cytogenetic register and the association of clinical cytogeneticists. J Med Genet 1996; 33: 387-94.
    • (1996) J Med Genet , vol.33 , pp. 387-394
    • Mutton, D.1    Alberman, E.2    Hook, E.B.3
  • 42
    • 3643070127 scopus 로고
    • Fragile X and other heritable fragile sites on human chromosomes
    • Barch MJ, ed. New York: Raven Press
    • Jacky P. Fragile X and other heritable fragile sites on human chromosomes. In: Barch MJ, ed. The ACT cytogentics laboratory manual. 2nd ed. New York: Raven Press, 1991: 489-523.
    • (1991) The ACT Cytogentics Laboratory Manual. 2nd Ed. , pp. 489-523
    • Jacky, P.1
  • 43
    • 0023099792 scopus 로고
    • Fragile sites still a mystery
    • Jordan BR. Fragile sites still a mystery. Lancet 1987; i: 497-8.
    • (1987) Lancet , vol.1 , pp. 497-498
    • Jordan, B.R.1
  • 45
    • 0028712179 scopus 로고
    • Fragile X syndrome
    • Laxova R. Fragile X syndrome. Adv Pediatr 1994; 41: 305-42.
    • (1994) Adv Pediatr , vol.41 , pp. 305-342
    • Laxova, R.1
  • 46
    • 0027606381 scopus 로고
    • Fragile site X chromosomes in mentally retarded boys
    • Moon HR, Moon SY. Fragile site X chromosomes in mentally retarded boys. J Korean Med Sci 1993; 8: 192-6.
    • (1993) J Korean Med Sci , vol.8 , pp. 192-196
    • Moon, H.R.1    Moon, S.Y.2
  • 47
    • 0023759213 scopus 로고
    • A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome
    • Li SY, Tsai CC, Chou MY, Lin JK. A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome. Hum Genet 1988; 79: 292-6.
    • (1988) Hum Genet , vol.79 , pp. 292-296
    • Li, S.Y.1    Tsai, C.C.2    Chou, M.Y.3    Lin, J.K.4
  • 48
    • 0026641068 scopus 로고
    • Fragile X positivity in Chinese children with autistic spectrum disorder
    • Wong VC, Lam ST. Fragile X positivity in Chinese children with autistic spectrum disorder. Pediatr Neurol 1992; 8: 272-4.
    • (1992) Pediatr Neurol , vol.8 , pp. 272-274
    • Wong, V.C.1    Lam, S.T.2
  • 50
    • 0023747113 scopus 로고
    • The fragile X-chromosome: An evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986
    • Veenema H, Beverstock GC, de Koning T, Pearson PL, van de Kamp JJ. The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986. Clin Genet 1988; 33: 410-7.
    • (1988) Clin Genet , vol.33 , pp. 410-417
    • Veenema, H.1    Beverstock, G.C.2    De Koning, T.3    Pearson, P.L.4    Van De Kamp, J.J.5
  • 51
  • 53
    • 0023925498 scopus 로고
    • The EEG in early diagnosis of Angelman's (happy puppet) syndrome
    • Boyd SG, Harden A, Patton MA. The EEG in early diagnosis of Angelman's (happy puppet) syndrome. Eur J Pediatr 1988; 147: 503-13.
    • (1988) Eur J Pediatr , vol.147 , pp. 503-513
    • Boyd, S.G.1    Harden, A.2    Patton, M.A.3
  • 56
    • 0023146037 scopus 로고
    • Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding
    • Tengström C, Autio S. Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding. Clin Genet 1987; 31: 53-60.
    • (1987) Clin Genet , vol.31 , pp. 53-60
    • Tengström, C.1    Autio, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.