ADDITIONAL MANIFESTATIONS OF THE NEU-LAXOVA SYNDROME

被引:15
作者
TURKEL, SB [1 ]
EBBIN, AJ [1 ]
TOWNER, JW [1 ]
机构
[1] UNIV SO CALIF,LOS ANGELES CTY MED CTR,DEPT PEDIAT,LOS ANGELES,CA 90033
关键词
D O I
10.1136/jmg.20.3.227
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:227 / 229
页数:3
相关论文
共 8 条
[1]  
CURRY CJR, 1981, CLIN RES, V29, pA130
[2]   FAMILIAL NORMAL/PARTIAL TRISOMY-16 WITH SELECTIVE ENDOREDUPLICATION IN MALFORMED PROBAND [J].
DRETS, ME ;
CARDOSO, JH ;
DELFINO, AH ;
CARRAU, J .
CYTOGENETICS, 1970, 9 (05) :333-&
[3]  
GENNADY IL, 1979, AM J MED GENET, V3, P261
[4]  
JORDE LB, 1982, HUM BIOL, V54, P583
[5]  
LAXOVA R, 1972, J MENT DEFIC RES, V16, P139
[6]   HERITABLE FRAGILE SITE ON CHROMOSOME-16 - PROBABLE LOCALIZATION OF HAPTOGLOBIN LOCUS IN MAN [J].
MAGENIS, RE ;
HECHT, F ;
LOVRIEN, EW .
SCIENCE, 1970, 170 (3953) :85-&
[7]  
NEU RL, 1971, PEDIATRICS, V47, P610
[8]  
Povysilova V, 1976, Cesk Pediatr, V31, P190