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Volumn 10, Issue 2, 1999, Pages 177-181

13q deletion syndrome in an adult mentally retarded patient

Author keywords

13q syndrome; Autosomal deletion; Chromosome 13

Indexed keywords

ADULT; ANUS ATRESIA; ARTICLE; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME DELETION 13; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; DIGESTIVE SYSTEM MALFORMATION; FINGER MALFORMATION; GROWTH RETARDATION; HUMAN; HUMAN CELL; KIDNEY MALFORMATION; LIMB MALFORMATION; MALE; MENTAL DEFICIENCY; RETINOBLASTOMA;

EID: 0032806855     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (13)
  • 1
    • 0022358901 scopus 로고
    • Sundareshan T.S. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32→qter
    • AL-AWADI S.A., TEEBI A.S.: Sundareshan T.S. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32→qter. Ann. Génét., 1985, 28, 181-184.
    • (1985) Ann. Génét. , vol.28 , pp. 181-184
    • Al-Awadi, S.A.1    Teebi, A.S.2
  • 2
    • 0027402372 scopus 로고
    • Preliminary definition of a «critical region» of chromosome 13 in q32: Report of 14 cases with 13q deletions and review of the literature
    • BROWN S., GERSEN S., ANYANE-YEBOA K., WARBURTON D.: Preliminary definition of a «critical region» of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature. Am. J. Med. Genet., 1993, 45, 52-59.
    • (1993) Am. J. Med. Genet. , vol.45 , pp. 52-59
    • Brown, S.1    Gersen, S.2    Anyane-Yeboa, K.3    Warburton, D.4
  • 3
    • 0028982746 scopus 로고
    • The 13q- syndrome: The molecular definition of a critical region in band 13q32
    • BROWN S., RUSSO J., CHITAYAT D., WARBURTON D.: The 13q- syndrome: the molecular definition of a critical region in band 13q32. Am. J. Hum. Genet., 1995, 57, 859-866.
    • (1995) Am. J. Hum. Genet. , vol.57 , pp. 859-866
    • Brown, S.1    Russo, J.2    Chitayat, D.3    Warburton, D.4
  • 7
    • 0015868352 scopus 로고
    • Ring chromosome D (13) associated with multiple congenital malformations
    • NIEBUHR E., OTTOSEN J.: Ring chromosome D (13) associated with multiple congenital malformations. Ann. Génét., 1973, 16, 157-166.
    • (1973) Ann. Génét. , vol.16 , pp. 157-166
    • Niebuhr, E.1    Ottosen, J.2
  • 8
    • 0003057157 scopus 로고
    • Partial trisomies and deletions of chromosome 13
    • J.J. Yunis (ed.). New York, Academic Press
    • NIEBUHR E.: Partial trisomies and deletions of chromosome 13. In: New Chromosomal Syndromes.J.J. Yunis (ed.). New York, Academic Press, 1977, 273-299.
    • (1977) New Chromosomal Syndromes , pp. 273-299
    • Niebuhr, E.1
  • 11
    • 0018885091 scopus 로고
    • Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32→qter
    • TELFER M.A., CLARK C.E., CASEY P.A., COWELL H.R., STROUD H.H.: Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32→qter. Clin. Genet., 1980, 17, 428-432.
    • (1980) Clin. Genet. , vol.17 , pp. 428-432
    • Telfer, M.A.1    Clark, C.E.2    Casey, P.A.3    Cowell, H.R.4    Stroud, H.H.5
  • 13
    • 0031568877 scopus 로고    scopus 로고
    • Characterisation of glypican-5 and chromosomal localisation of human GPC5 , a new member of the glypican gene family
    • VEUGELERS M., VERMEESCH J., REEKMANS G., STEINFELD R., MARYNEN P., DAVID G.: Characterisation of glypican-5 and chromosomal localisation of human GPC5 , a new member of the glypican gene family. Genomics, 1997, 40, 24-30.
    • (1997) Genomics , vol.40 , pp. 24-30
    • Veugelers, M.1    Vermeesch, J.2    Reekmans, G.3    Steinfeld, R.4    Marynen, P.5    David, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.