PREDICTING GENOTYPES AT LOCI FOR AUTOSOMAL RECESSIVE DISORDERS USING LINKED GENETIC-MARKERS - APPLICATION TO WILSONS-DISEASE

被引：17
作者：
FARRER, LA
BONNETAMIR, B
FRYDMAN, M
MAGAZANIK, A
KIDD, KK
BOWCOCK, AM
CAVALLISFORZA, LL
机构：
[1] BOSTON UNIV,SCH MED,MED CTR,SCH PUBL HLTH,BOSTON,MA 02118
[2] HARVARD UNIV,SCH MED,DEPT NEUROL,BOSTON,MA 02118
[3] TEL AVIV UNIV,SACKLER SCH MED,DEPT HUMAN GENET,TEL AVIV,ISRAEL
[4] HASHARON HOSP,DEPT PEDIAT & BIOCHEM,PETAH TIKVA,ISRAEL
[5] YALE UNIV,SCH MED,DEPT HUMAN GENET,NEW HAVEN,CT 06510
[6] STANFORD UNIV,DEPT GENET,STANFORD,CA 94305
来源：
HUMAN GENETICS | 1988年 / 79卷 / 02期
关键词：
D O I：
10.1007/BF00280547
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：109 / 117
页数：9
相关论文
共 44 条
[1]   WILSON DISEASE OF THE BRAIN - MR IMAGING [J].
AISEN, AM ;
MARTEL, W ;
GABRIELSEN, TO ;
GLAZER, GM ;
BREWER, G ;
YOUNG, AB ;
HILL, G .
RADIOLOGY, 1985, 157 (01) :137-141
[2]   DUCHEN - AN INTERACTIVE COMPUTER-PROGRAM FOR CALCULATING HETEROZYGOSITY (CARRIER) RISKS IN X-LINKED RECESSIVE LETHAL DISEASES, AND ITS APPLICATION IN DUCHENNE MUSCULAR-DYSTROPHY [J].
ANDREWS, DF ;
BRASHER, PMA ;
MANCHESTER, KE ;
PERCY, ME ;
RUSK, ACM ;
SOLTAN, HC ;
TRUEMAN, DW .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 25 (02) :211-218
[3]  
ARIMA M, 1968, Birth Defects Original Article Series, V4, P54
[4]   EVIDENCE FOR LINKAGE BETWEEN WILSON DISEASE AND ESTERASE-D IN 3 KINDREDS - DETECTION OF LINKAGE FOR AN AUTOSOMAL RECESSIVE DISORDER BY THE FAMILY STUDY METHOD [J].
BONNETAMIR, B ;
FARRER, LA ;
FRYDMAN, M ;
KANAANEH, H .
GENETIC EPIDEMIOLOGY, 1986, 3 (03) :201-209
[5]   A NEW HUMAN RFLP IDENTIFIED BY 7D2 PLACES D13S10 PROXIMAL TO ESTERASE-D [J].
BOWCOCK, AM ;
FARRER, LA ;
HEBERT, JM ;
BONNETAMIR, B ;
FRYDMAN, M ;
KIDD, KK ;
CAVALLISFORZA, LL .
CYTOGENETICS AND CELL GENETICS, 1987, 44 (04) :236-237
[6]  
BOWCOCK AM, 1987, AM J HUM GENET, V41, P27
[7]  
CHAKRAVARTI A, 1982, AM J HUM GENET, V34, P531
[8]  
COX DW, 1985, CYTOGENET CELL GENET, V40, P608
[9]  
COX DW, 1966, J LAB CLIN MED, V68, P893
[10]  
COX DW, 1972, AM J HUM GENET, V24, P646
12345