HOMOZYGOSITY MAPPING AND WERNERS SYNDROME

被引：62

作者：

SCHELLENBERG, GD

MARTIN, GM

WIJSMAN, EM

NAKURA, J

MIKI, T

OGIHARA, T

机构：

[1] UNIV WASHINGTON,DEPT PATHOL,SEATTLE,WA 98195

[2] UNIV WASHINGTON,DEPT MED GENET,SEATTLE,WA 98195

[3] OSAKA UNIV,DEPT GERIATR MED,OSAKA,JAPAN

来源：

LANCET | 1992年 / 339卷 / 8799期

关键词：

D O I：

10.1016/0140-6736(92)91590-5

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1002 / 1002

页数：1

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[2]

DEAN G, 1988, LANCET, V1, P587

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EPSTEIN, CJ ;

MARTIN, GM ;

SCHULTZ, AL ;

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MEDICINE, 1966, 45 (03) :177-+

[4] GENETIC-LINKAGE OF WERNER SYNDROME TO 5 MARKERS ON CHROMOSOME-8 [J].

GOTO, M ;

RUBENSTEIN, M ;

WEBER, J ;

WOODS, K ;

DRAYNA, D .

NATURE, 1992, 355 (6362) :735-738

[5] HOMOZYGOSITY MAPPING - A WAY TO MAP HUMAN RECESSIVE TRAITS WITH THE DNA OF INBRED CHILDREN [J].

LANDER, ES ;

BOTSTEIN, D .

SCIENCE, 1987, 236 (4808) :1567-1570

[6]

Martin G M, 1978, Birth Defects Orig Artic Ser, V14, P5

[7]

SMITH CAB, 1953, J R STAT SOC B, V15, P153

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