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Volumn 33, Issue 1, 2003, Pages 105-108

Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3)

Author keywords

Autism; Chromosome 2q; Cytogenetics; Genetics

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 2; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; GENETIC LINKAGE; HEREDITY; HUMAN; LINKAGE ANALYSIS; MALE; PRIORITY JOURNAL;

EID: 0037296086     PISSN: 01623257     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1022242807513     Document Type: Article
Times cited : (21)

References (21)
  • 3
    • 0022467685 scopus 로고
    • Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46, XX, del (2)(q31q33)
    • Benson, K., Gordon, M., Wassman, E. R., & Tsi C. (1986). Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46, XX, del (2)(q31q33). American Journal of Medical Genetics 25, 405-411.
    • (1986) American Journal of Medical Genetics , vol.25 , pp. 405-411
    • Benson, K.1    Gordon, M.2    Wassman, E.R.3    Tsi, C.4
  • 6
    • 0033573212 scopus 로고    scopus 로고
    • An autosomal genomic screen for autism
    • Collaborative Linkage Study of Autism. (1999). An autosomal genomic screen for autism. American Journal of Medical Genetics, 88, 609-615.
    • (1999) American Journal of Medical Genetics , vol.88 , pp. 609-615
  • 7
    • 0020959116 scopus 로고
    • Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation
    • Franceschini, P., Silengo, M., Davi, G., Bianco, R., Biagiolo, M. (1983). Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation. Human Genetics, 64, 98.
    • (1983) Human Genetics , vol.64 , pp. 98
    • Franceschini, P.1    Silengo, M.2    Davi, G.3    Bianco, R.4    Biagiolo, M.5
  • 9
    • 6844251000 scopus 로고    scopus 로고
    • A full geneome screen for autism with evidence for linkage to a region on chromosome 7q
    • International Molecular Genetic Study of Autism Consortium. (1998). A full geneome screen for autism with evidence for linkage to a region on chromosome 7q. Human Molecular Genetics 7, 571-578.
    • (1998) Human Molecular Genetics , vol.7 , pp. 571-578
  • 10
    • 0034883367 scopus 로고    scopus 로고
    • A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q and 16p
    • International Molecular Genetic Study of Autism Consortium. (2001). A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q and 16p. American Journal of Human Genetics, 69, 570-581.
    • (2001) American Journal of Human Genetics , vol.69 , pp. 570-581
  • 11
    • 0000984981 scopus 로고
    • Autistic disturbances of affective contact
    • Kanner, L. (1943) Autistic disturbances of affective contact. Nerv. Child, 2, 217-250.
    • (1943) Nerv Child , vol.2 , pp. 217-250
    • Kanner, L.1
  • 14
    • 0020673351 scopus 로고
    • Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del (2)(q32) in two sisters with intrachromosomal insertional translocation in their father
    • Pai, G. S., Rogers, J. F., & Sommer, A. (1983). Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del (2)(q32) in two sisters with intrachromosomal insertional translocation in their father. American Journal of Medical Genetics, 14, 189-195.
    • (1983) American Journal of Medical Genetics , vol.14 , pp. 189-195
    • Pai, G.S.1    Rogers, J.F.2    Sommer, A.3
  • 16
    • 0025110206 scopus 로고
    • Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: Review of brain, cardiac and limb formations
    • Ramer, J. C., Mowrey, P. N., Robins, D. B., Ligato, S., Towfighi, J., & Ladda, R. L. (1990). Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: Review of brain, cardiac and limb formations. American Journal of Medical Genetics, 37, 392-400.
    • (1990) American Journal of Medical Genetics , vol.37 , pp. 392-400
    • Ramer, J.C.1    Mowrey, P.N.2    Robins, D.B.3    Ligato, S.4    Towfighi, J.5    Ladda, R.L.6
  • 17
    • 0033362024 scopus 로고    scopus 로고
    • A genomic screen of autism: Evidence for a multilocus etiology
    • Risch et al. (1999). A genomic screen of autism: Evidence for a multilocus etiology. American Journal of Human Genetics, 65, 493-507.
    • (1999) American Journal of Human Genetics , vol.65 , pp. 493-507
    • Risch1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.