RING CHROMOSOME-11 AND CAFE-AU-LAIT SPOTS

被引:24
作者
FAGAN, K
SUTHERS, GK
HARDACRE, G
机构
[1] PRINCE WALES CHILDRENS HOSP,DEPT MED GENET,RANDWICK,NSW,AUSTRALIA
[2] CHILD DEV UNIT,HAMILTON,NSW,AUSTRALIA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 30卷 / 04期
关键词
D O I
10.1002/ajmg.1320300406
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:911 / 916
页数:6
相关论文
共 19 条
[1]   GENE FOR VON RECKLINGHAUSEN NEUROFIBROMATOSIS IS IN THE PERICENTROMERIC REGION OF CHROMOSOME-17 [J].
BARKER, D ;
WRIGHT, E ;
NGUYEN, K ;
CANNON, L ;
FAIN, P ;
GOLDGAR, D ;
BISHOP, DT ;
CAREY, J ;
BATY, B ;
KIVLIN, J ;
WILLARD, H ;
WAYE, JS ;
GREIG, G ;
LEINWAND, L ;
NAKAMURA, Y ;
OCONNELL, P ;
LEPPERT, M ;
LALOUEL, JM ;
WHITE, R ;
SKOLNICK, M .
SCIENCE, 1987, 236 (4805) :1100-1102
[2]  
Bowser-Riley S, 1981, J MED GENET, V18, P209
[3]  
Burden M, 1973, Rev Med Chir Soc Med Nat Iasi, V77, P353
[4]  
CHRISTENSEN KR, 1970, J MENT DEFIC RES, V14, P54
[5]   RING CHROMOSOME-21 IN HEALTHY-PERSONS - DIFFERENT CONSEQUENCES IN FEMALES AND IN MALES [J].
DALLAPICCOLA, B ;
DEFILIPPIS, V ;
NOTARANGELO, A ;
PERLA, G ;
ZELANTE, L .
HUMAN GENETICS, 1986, 73 (03) :218-220
[6]   CONGENITAL OCULAR AND OTHER SYSTEMIC ABNORMALITIES ASSOCIATED WITH RING-11 CHROMOSOME [J].
DANIELE, S ;
PECORELLI, F ;
TIEPOLO, L ;
ARMELLINI, R ;
LIOTTI, FS .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 1986, 224 (03) :317-320
[7]   RING CHROMOSOME-18 IN A MOTHER AND SON [J].
DONLAN, MA ;
DOLAN, CR .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (01) :171-174
[8]   NEUROFIBROMATOSIS IN A MAN WITH A RING-22 - INSITU HYBRIDIZATION STUDIES [J].
DUNCAN, AMV ;
PARTINGTON, MW ;
SOUDEK, D .
CANCER GENETICS AND CYTOGENETICS, 1987, 25 (01) :169-174
[9]   RING CHROMOSOME-22 IN A MENTALLY-RETARDED CHILD AND MOSAIC 45,XX,-15,-22,+T(15-22)(P11-Q11)-46,XX,R(22)-46,XX KARYOTYPE IN THE MOTHER [J].
FRYNS, JP ;
VANDENBERGHE, H .
HUMAN GENETICS, 1979, 47 (02) :213-216
[10]   OCCURRENCE OF A RING-18, AN ACCESSORY BISATELLITED FRAGMENT, AND TRISOMY-21 WITHIN ONE SIBSHIP [J].
GRACE, E ;
SILLS, J .
HUMAN GENETICS, 1978, 43 (01) :111-114