메뉴 건너뛰기




Volumn 123 A, Issue 2, 2003, Pages 201-203

Ring Chromosome 10 (p15q26) in a Patient with Unipolar Affective Disorder, Multiple Minor Anomalies, and Mental Retardation [4]

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANXIETY DISORDER; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOME 10Q; CLINICAL FEATURE; CRYPTORCHISM; DEPENDENT PERSONALITY DISORDER; DEPRESSION; FEEDING DISORDER; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 46,XY; LETTER; MAJOR DEPRESSION; MALE; MENTAL DEFICIENCY; OBSESSION; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; RING CHROMOSOME;

EID: 0242426664     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (6)

References (18)
  • 3
  • 4
    • 0037040472 scopus 로고    scopus 로고
    • Search for a shared segment on chromosome 10q26 in patient with bipolar affective disorder or schizophrenia from Faroe Island
    • Ewald H, Flint TJ, Jorgensen TH, Wang AG, Jensen P, Vang M, Mors O, Kruse TA. 2002. Search for a shared segment on chromosome 10q26 in patient with bipolar affective disorder or schizophrenia from Faroe Island. Am J Med Genet 114(2):196-204.
    • (2002) Am J Med Genet , vol.114 , Issue.2 , pp. 196-204
    • Ewald, H.1    Flint, T.J.2    Jorgensen, T.H.3    Wang, A.G.4    Jensen, P.5    Vang, M.6    Mors, O.7    Kruse, T.A.8
  • 5
    • 0017816140 scopus 로고
    • Malformative syndrome associated with a ring 10 chromosome and translocated 10q/19 chromosome
    • Fryns P, De Boeck K, Jaken J, van der Berg H. 1978. Malformative syndrome associated with a ring 10 chromosome and translocated 10q/19 chromosome. Hum Genet 43:239-244.
    • (1978) Hum Genet , vol.43 , pp. 239-244
    • Fryns, P.1    De Boeck, K.2    Jaken, J.3    Van Der Berg, H.4
  • 6
    • 0023912059 scopus 로고    scopus 로고
    • Behavioural disorders in the mentally handicapped. The role of life events
    • Ghaziuddin M. 1998. Behavioural disorders in the mentally handicapped. The role of life events. Brit J Psychiat 152:683-686.
    • (1998) Brit J Psychiat , vol.152 , pp. 683-686
    • Ghaziuddin, M.1
  • 7
    • 0033173068 scopus 로고    scopus 로고
    • Chromosomal abnormalities in child psychiatric patients
    • Hong KE, Kim JH, Moon SY, Oh SK. 1999. Chromosomal abnormalities in child psychiatric patients. J Korean Med Sci 14(4):377-385.
    • (1999) J Korean Med Sci , vol.14 , Issue.4 , pp. 377-385
    • Hong, K.E.1    Kim, J.H.2    Moon, S.Y.3    Oh, S.K.4
  • 9
    • 0034122180 scopus 로고    scopus 로고
    • Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence
    • Lukusa T, Fryns JP. 2000. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence. Genet Couns 11(2):119-126.
    • (2000) Genet Couns , vol.11 , Issue.2 , pp. 119-126
    • Lukusa, T.1    Fryns, J.P.2
  • 10
    • 0023114615 scopus 로고
    • Behaviour disorder in monosomy 10qter
    • Metha L, Duckett DP, Young ID. 1987. Behaviour disorder in monosomy 10qter. J Med Genet 24:185-187.
    • (1987) J Med Genet , vol.24 , pp. 185-187
    • Metha, L.1    Duckett, D.P.2    Young, I.D.3
  • 11
    • 0141742090 scopus 로고    scopus 로고
    • Mental disorders and problematic behaviours in people with intellectual disability: Future directions for research
    • Moss S, Emerson E, Bouras N, Holland A. 1997. Mental disorders and problematic behaviours in people with intellectual disability: Future directions for research. J Intellect Disabil Res 41:440-447.
    • (1997) J Intellect Disabil Res , vol.41 , pp. 440-447
    • Moss, S.1    Emerson, E.2    Bouras, N.3    Holland, A.4
  • 12
    • 0032446794 scopus 로고    scopus 로고
    • Terminal deletion of chromosome 10q26: Delineation of two clinical phenotypes
    • Petit P, Devriendt K, Azou M, Gewilling M, Fryns P. 1998. Terminal deletion of chromosome 10q26: Delineation of two clinical phenotypes. Genet Counsel 4:271-475.
    • (1998) Genet Counsel , vol.4 , pp. 271-475
    • Petit, P.1    Devriendt, K.2    Azou, M.3    Gewilling, M.4    Fryns, P.5
  • 13
    • 0024207766 scopus 로고
    • A systematic cytogenetic study of a population of 1,170 mental retarded and/or behaviourly disturbed patients including fraX-screening. The Hondsberg experience
    • Schreppers-Tijdink GA, Curfs LM, Wiegers A, Kleczowska A, Fryns JP. 1988. A systematic cytogenetic study of a population of 1,170 mental retarded and/or behaviourly disturbed patients including fraX-screening. The Hondsberg experience. J Genet Hum 36(5):425-446.
    • (1988) J Genet Hum , vol.36 , Issue.5 , pp. 425-446
    • Schreppers-Tijdink, G.A.1    Curfs, L.M.2    Wiegers, A.3    Kleczowska, A.4    Fryns, J.P.5
  • 15
    • 0017814339 scopus 로고
    • Ring 10 chromosome: 46,XX, r10 (p15q26)
    • Sparkes RS, Ling SM, Muller H. 1978. Ring 10 chromosome: 46,XX, r10 (p15q26). Hum Genet 43:341-345.
    • (1978) Hum Genet , vol.43 , pp. 341-345
    • Sparkes, R.S.1    Ling, S.M.2    Muller, H.3
  • 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.