3-POINT LINKAGE ANALYSIS EMPLOYING C-3 AND 19CEN MARKERS ASSIGNS THE MYOTONIC-DYSTROPHY GENE TO 19Q

被引:43
作者
FRIEDRICH, U
BRUNNER, H
SMEETS, D
LAMBERMON, E
ROPERS, HH
机构
[1] CATHOLIC UNIV NIJMEGEN,INST ANTHROPOGENET,DEPT HUMAN GENET,GEERT GROOTEPLEIN ZUID 20,6525 GA NIJMEGEN,NETHERLANDS
[2] AARHUS UNIV,INST HUMAN GENET,DK-8000 AARHUS C,DENMARK
关键词
D O I
10.1007/BF00281077
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:291 / 293
页数:3
相关论文
共 17 条
[1]  
BALL SP, 1984, BIRTH DEFECTS-ORIG, V20, P411
[2]  
EIBERG H, 1983, CLIN GENET, V24, P159
[3]  
FRIEDRICH U, 1985, CLIN GENET, V28, P358
[4]  
HARPER PS, 1972, THESIS U OXFORD UK
[5]  
HULSEBOS T, 1985, CYTOGENET CELL GENET, V40, P658
[6]   TOWARD EARLY DIAGNOSIS OF MYOTONIC-DYSTROPHY - CONSTRUCTION AND CHARACTERIZATION OF A SOMATIC-CELL HYBRID WITH A SINGLE HUMAN DER(19) CHROMOSOME [J].
HULSEBOS, T ;
WIERINGA, B ;
HOCHSTENBACH, R ;
SMEETS, D ;
SCHEPENS, J ;
OERLEMANS, F ;
ZIMMER, J ;
ROPERS, HH .
CYTOGENETICS AND CELL GENETICS, 1986, 43 (1-2) :47-56
[7]  
HULTEN M, 1974, HEREDITAS, V76, P52
[8]  
LUSIS AJ, 1985, CYTOGENET CELL GENET, V40, P683
[9]  
MEREDITH AL, 1985, CYTOGENET CELL GENET, V40, P698
[10]  
MOHR J, 1951, ACTA PATHOL MIC SC, V29, P339