PARTIAL 12P DELETION - CAUSE FOR A MENTAL-RETARDATION, MULTIPLE CONGENITAL ABNORMALITY SYNDROME

被引:22
作者
MAGNELLI, NC [1 ]
THERMAN, E [1 ]
机构
[1] UNIV WISCONSIN,DEPT MED GENET,MADISON,WI 53706
关键词
D O I
10.1136/jmg.12.1.105
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:105 / 108
页数:4
相关论文
共 9 条
[1]  
BOCHKOV N P, 1969, Genetica (Dordrecht), V5, P108
[2]   CYTOLOGICAL STUDIES ON A HUMAN RING CHROMOSOME [J].
COOKE, P ;
GORDON, RR .
ANNALS OF HUMAN GENETICS, 1965, 29 :147-&
[3]  
HECHT F, 1969, Birth Defects Original Article Series, V5, P106
[4]  
HSU T. C., 1963, EXPTL CELL RES SUPPL, V9, P73, DOI 10.1016/0014-4827(63)90246-5
[5]  
LAURENT C, 1968, ANN GENET-PARIS, V11, P231
[6]  
MAGNELLI NC, IN PRESS
[7]  
PATAU K, 1965, BIRTH DEFECTS OAS 1, V1, P71
[8]   CYTOGENETICS IN MENTALLY DEFECTIVE CHILDREN WITH ANOMALIES - A CONTROLLED STUDY [J].
SUMMITT, RL .
JOURNAL OF PEDIATRICS, 1969, 74 (01) :58-+
[9]  
UCHIDA IA, 1965, AM J HUM GENET, V17, P410