4 DNA POLYMORPHISMS IN THE LDL RECEPTOR GENE - THEIR GENETIC-RELATIONSHIP AND USE IN THE STUDY OF VARIATION AT THE LDL RECEPTOR LOCUS

被引：39
作者：
TAYLOR, R [1 ]
JEENAH, M [1 ]
SEED, M [1 ]
HUMPHRIES, S [1 ]
机构：
[1] CHARING CROSS HOSP MED SCH,LONDON W6 8RF,ENGLAND
来源：
JOURNAL OF MEDICAL GENETICS | 1988年 / 25卷 / 10期
关键词：
D O I：
10.1136/jmg.25.10.653
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：653 / 659
页数：7
相关论文
共 39 条
[11]   DELETION IN THE GENE FOR THE LOW-DENSITY-LIPOPROTEIN RECEPTOR IN A MAJORITY OF FRENCH-CANADIANS WITH FAMILIAL HYPERCHOLESTEROLEMIA [J].
HOBBS, HH ;
BROWN, MS ;
RUSSELL, DW ;
DAVIGNON, J ;
GOLDSTEIN, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (12) :734-737
[12]   UNEQUAL CROSSING-OVER BETWEEN 2 ALU-REPETITIVE DNA-SEQUENCES IN THE LOW-DENSITY-LIPOPROTEIN-RECEPTOR GENE - A POSSIBLE MECHANISM FOR THE DEFECT IN A PATIENT WITH FAMILIAL HYPERCHOLESTEROLEMIA [J].
HORSTHEMKE, B ;
BEISIEGEL, U ;
DUNNING, A ;
HAVINGA, JR ;
WILLIAMSON, R ;
HUMPHRIES, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 164 (01) :77-81
[13]   IDENTIFICATION OF DELETIONS IN THE HUMAN LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE [J].
HORSTHEMKE, B ;
DUNNING, A ;
HUMPHRIES, S .
JOURNAL OF MEDICAL GENETICS, 1987, 24 (03) :144-147
[14]  
HUMPHRIES SE, 1985, LANCET, V1, P1003
[15]   THE USE OF POLYMORPHIC DNA AND PROTEIN MARKERS FOR THE 3RD COMPLEMENT COMPONENT FOR DETERMINING LINKAGE OF FAMILIAL HYPERCHOLESTEROLEMIA [J].
HUMPHRIES, SE ;
DONALD, JA ;
MCFADDEN, JJP ;
SHULL, S ;
WILLIAMSON, R ;
JOWETT, NI ;
GALTON, DJ ;
JULSRUD, JO ;
BERG, K ;
HEIBERG, A ;
BALL, S ;
FEY, G ;
SEED, M ;
WYNN, V .
ATHEROSCLEROSIS, 1984, 52 (03) :267-278
[16]  
KESSLING AM, 1988, AM J HUM GENET, V42, P458
[17]  
KESSLING AM, UNPUB RISING CHOLEST
[18]   A RFLP ASSOCIATED WITH THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE (LDLR) [J].
KOTZE, MJ ;
LANGENHOVEN, E ;
DIETZSCH, E ;
RETIEF, AE .
NUCLEIC ACIDS RESEARCH, 1987, 15 (01) :376-376
[19]  
KOTZE MJ, 1986, S AFR MED J, V70, P77
[20]  
LAW A, 1986, LANCET, V1, P1301
1234