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Volumn 25, Issue 4, 1988, Pages 260-262

De Novo partial trisomy 15q (proximal type)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHILD; CHROMOSOME 15Q; CYTOLOGY; HEREDITY; HUMAN; MENTAL RETARDATION MALFORMATION SYNDROME; PARTIAL TRISOMY 15;

EID: 0023943165     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.25.4.260     Document Type: Article
Times cited : (7)

References (22)
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    • Parker, C.E.1    Alfi, O.S.2
  • 3
    • 0015590068 scopus 로고
    • Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding
    • Crandall, B.F.; Mullier, H.M.; Bass, H.N. Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding Am J Ment Defic 1973 77 571
    • (1973) Am J Ment Defic , vol.77 , pp. 571
    • Crandall, B.F.1    Mullier, H.M.2    Bass, H.N.3
  • 5
    • 0016311860 scopus 로고
    • A case of partial trisomy
    • Watson, E.J.; Gordon, R.R. A case of partial trisomy 15. J Med Genet 1974 10.1136/jmg.11.4.400 11 400
    • (1974) 15. J Med Genet , vol.11 , pp. 400
    • Watson, E.J.1    Gordon, R.R.2
  • 7
    • 0017147938 scopus 로고
    • Partial trisomy 15ql
    • Pfeiffer, R.A.; Kessel, E. Partial trisomy 15ql Hum Genet 1976 10.1007/BF00447290 33 77
    • (1976) Hum Genet , vol.33 , pp. 77
    • Pfeiffer, R.A.1    Kessel, E.2
  • 8
    • 0018395580 scopus 로고
    • Partial trisomy 15 and intractable seizures
    • Taysi, K.; Devivo, D.C.; Sekhon, G.S. Partial trisomy 15 and intractable seizures Acta Paediatr Scand 1979 10.1111/j.1651-2227.1979.tb05036.x 68 445
    • (1979) Acta Paediatr Scand , vol.68 , pp. 445
    • Taysi, K.1    Devivo, D.C.2    Sekhon, G.S.3
  • 9
    • 0017870782 scopus 로고
    • Modification of DAPI banding on human chromosomes by prestaining with a DNAbinding oligopeptide antibiotic, distamycin A
    • Schweizer, D.; Ambos, P.; Anderle, M. Modification of DAPI banding on human chromosomes by prestaining with a DNAbinding oligopeptide antibiotic, distamycin A Exp Cell Res 1978 10.1016/0014-4827(78)90177-5 111 327
    • (1978) Exp Cell Res , vol.111 , pp. 327
    • Schweizer, D.1    Ambos, P.2    Anderle, M.3
  • 10
    • 85142976498 scopus 로고
    • The human gene map 1
    • McKusick, V.A. The human gene map 1 1984 Clin Genet 27 207
    • (1984) Clin Genet , vol.27 , pp. 207
    • McKusick, V.A.1
  • 11
    • 85142942096 scopus 로고
    • Translocation 46, XX, t (15; 21) (ql3; q22,1) chez la mere de deux enfants atteints de trisomie 15 et de monosomie 21 partielles
    • Rethor6, M.; Dutrillaux, B.; Lejeune, J. Translocation 46, XX, t (15; 21) (ql3; q22,1) chez la mere de deux enfants atteints de trisomie 15 et de monosomie 21 partielles Ann Genet (Paris) 1973 16 271-5
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    • Rethor6, M.1    Dutrillaux, B.2    Lejeune, J.3
  • 12
    • 84913688802 scopus 로고
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    • Breg, W.R.; Schreck, R.R.; Miller, O.J. Familial partial trisomy 15: identification of a deleted no 15 confirmed by anti-5-methylcytodine antibody binding Am J Hum Genet 1974 26 17
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    • Breg, W.R.1    Schreck, R.R.2    Miller, O.J.3
  • 13
    • 0016741795 scopus 로고
    • A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange
    • Bannister, D.L.; Engel, E. A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange J Pediatr 1975 10.1016/S0022-3476(75)80228-9 86 916
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    • Bannister, D.L.1    Engel, E.2
  • 15
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  • 18
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  • 19
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.