SPECTRUM OF ANOMALIES IN FANCONI ANEMIA

被引:148
作者
GLANZ, A
FRASER, FC
机构
[1] MONTREAL CHILDRENS HOSP, DEPT MED GENET, MONTREAL H3H 1P3, QUEBEC, CANADA
[2] MCGILL UNIV, DEPT BIOL, MONTREAL H3A 1B1, QUEBEC, CANADA
[3] MCGILL UNIV, CTR HUMAN GENET, MONTREAL H3A 1B1, QUEBEC, CANADA
关键词
D O I
10.1136/jmg.19.6.412
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:412 / 416
页数:5
相关论文
共 54 条
[1]  
AHJUJA BK, 1969, INDIAN J PEDIATR, V36, P284
[2]  
ALTAY C, 1975, NEW ENGL J MED, V293, P151
[3]  
AUERBACH AD, 1979, AM J HUM GENET, V31, P77
[4]   NONRANDOM DISTRIBUTION OF CHROMOSOME BREAKS IN CULTURED LYMPHOCYTES OF NORMAL SUBJECTS [J].
AYME, S ;
MATTEI, JF ;
MATTEI, MG ;
AURRAN, Y ;
GIRAUD, F .
HUMAN GENETICS, 1976, 31 (02) :161-175
[5]   STUDIES OF MALFORMATION SYNDROMES OF MAN .47. DISAPPEARANCE OF SPERMATOGONIA IN FANCONI ANEMIA SYNDROME [J].
BARGMAN, GJ ;
SHAHIDI, NT ;
GILBERT, EF ;
OPITZ, JM .
EUROPEAN JOURNAL OF PEDIATRICS, 1977, 125 (03) :163-168
[6]  
BERGER R, 1975, NOUV REV FR HEMATOL, V15, P539
[7]  
BERGER R, 1977, CLIN GENET, V11, P409
[8]  
BLOOM GE, 1972, PEDIATR CLIN N AM, V19, P983
[9]  
BUSHKELL LL, 1976, CLIN GENET, V9, P583
[10]   CONGENITAL HYPOPLASTIC ANEMIA ASSOCIATED WITH MULTIPLE DEVELOPMENTAL DEFECTS (FANCONIS SYNDROME) [J].
CASSIMOS, C ;
ZANNOS, L .
AMA AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1952, 84 (03) :347-350