TRISOMY-8 SYNDROME

被引：22
|
作者：
TUNCBILEK, E [1 ]
HALICIOGLU, C [1 ]
SAY, B [1 ]
机构：
[1] HACETTEPE UNIV, DEPT PEDIAT, DIV CLIN GENET, ANKARA, TURKEY
来源：
HUMANGENETIK | 1974年 / 23卷 / 01期
关键词：
D O I：
10.1007/BF00295679
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：23 / 29
页数：7
相关论文
共 50 条
  • [41] ATYPICAL CHRONIC MYELOGENOUS LEUKEMIA IN A PATIENT WITH TRISOMY-8 MOSAICISM SYNDROME
    KAPAUN, P
    KABISCH, H
    HELD, KR
    WALTER, TA
    HEGEWISCH, S
    ZANDER, AR
    ANNALS OF HEMATOLOGY, 1993, 66 (01) : 57 - 58
  • [42] RADIOGRAPHIC FEATURES OF TRISOMY-8 MOSAICISM
    SMITH, LE
    CRANDALL, BF
    BASS, HN
    GYEPES, MT
    CLINICAL RESEARCH, 1976, 24 (02): : A172 - A172
  • [43] 2 CASES OF TRISOMY-8 MOSAICISM
    KONDO, I
    JAPANESE JOURNAL OF HUMAN GENETICS, 1976, 21 (01): : 5 - 11
  • [44] PARTIAL TRISOMY-8 (TRISOMY 8Q2106-]8QTER)
    ABUELO, D
    PERL, DP
    HENKLE, C
    RICHARDSON, A
    JOURNAL OF MEDICAL GENETICS, 1977, 14 (06) : 463 - 466
  • [45] ACUTE-LEUKEMIA CHARACTERIZED BY TRISOMY-8 IN DOWNS-SYNDROME
    BROOMHEAD, AF
    KWAN, YL
    ZELL, NA
    LAMPOTANG, PRL
    HUGHES, DOG
    PATHOLOGY, 1985, 17 (01) : 111 - 114
  • [46] MYELODYSPLASTIC SYNDROME WITH TRISOMY-8 IN AN ADOLESCENT WITH FANCONI ANEMIA AND SELECTIVE IGA DEFICIENCY
    STANDEN, GR
    HUGHES, IA
    GEDDES, AD
    JONES, BM
    WARDROP, CAJ
    AMERICAN JOURNAL OF HEMATOLOGY, 1989, 31 (04) : 280 - 283
  • [47] SOME DESMOID TUMORS ARE CHARACTERIZED BY TRISOMY-8
    DALCIN, P
    SCIOT, R
    ALY, MS
    DELABIE, J
    STAS, M
    DEWEVER, I
    VANDAMME, B
    VANDENBERGHE, H
    GENES CHROMOSOMES & CANCER, 1994, 10 (02): : 131 - 135
  • [48] HYPEREOSINOPHILIC SYNDROME IN CHILDHOOD - TRISOMY-8 AND TRANSFORMATION TO MIXED ACUTE-LEUKEMIA
    GUITARD, AM
    HORSCHOWSKI, N
    MOZZICONACCI, MJ
    MICHEL, G
    GEORGE, F
    CAPODANO, AM
    PERRIMOND, H
    NOUVELLE REVUE FRANCAISE D HEMATOLOGIE, 1993, 35 (06): : 555 - 559
  • [49] MYELODYSPLASTIC-SYNDROME IN A CHILD WITH CONSTITUTIONAL TRISOMY-8 MOSAICISM AND NORMAL PHENOTYPE
    HASLE, H
    CLAUSEN, N
    PEDERSEN, B
    BENDIXHANSEN, K
    CANCER GENETICS AND CYTOGENETICS, 1995, 79 (01) : 79 - 81
  • [50] TRISOMY-8 SYNDROME - THE RIB ANOMALY AND SOME NEW FEATURES IN 2 CASES
    ANNEREN, G
    FRODIS, E
    JORULF, H
    HELVETICA PAEDIATRICA ACTA, 1981, 36 (05) : 465 - 472
12345