GENETIC-HETEROGENEITY OF ALPORT SYNDROME

被引：181

作者：

FEINGOLD, J

BOIS, E

CHOMPRET, A

BROYER, M

GUBLER, MC

GRUNFELD, JP

机构：

[1] HOP NECKER,DEPT NEPHROL,F-75730 PARIS 15,FRANCE

[2] INSERM,UNITE 192,DEPT PEDIAT NEPHROL,F-75005 PARIS,FRANCE

来源：

KIDNEY INTERNATIONAL | 1985年 / 27卷 / 04期

关键词：

D O I：

10.1038/ki.1985.63

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：672 / 677

页数：6

共 18 条

[1]

COHEN MM, 1961, AM J HUM GENET, V13, P379

[2]

EVANS SH, 1980, CLIN GENET, V17, P285

[3] GENETICS OF ALPORT SYNDROME - HEREDITARY NEPHROPATHY WITH DEAFNESS [J].

FEINGOLD, J .

HUMANGENETIK, 1971, 12 (01) :29-+

[4] DAS SYNDROM DER ERBLICHEN NEPHROPATHIE MIT INNENOHRSCHWERHORIGKEIT (ALPORT-SYNDROM) [J].

FUHRMANN, W .

DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1963, 88 (11) :525-+

[5]

GRAHAM JB, 1959, AM J HUM GENET, V11, P333

[6] PROGRESSIVE AND NONPROGRESSIVE HEREDITARY CHRONIC NEPHRITIS [J].

GRUNFELD, JP ;

BOIS, EP ;

HINGLAIS, N .

KIDNEY INTERNATIONAL, 1973, 4 (03) :216-228

[7]

HABIB R, 1982, KIDNEY INT S11, V21, P20

[8] The relative importance of principal and modifying genes in determining some human diseases [J].

Haldane, JBS .

JOURNAL OF GENETICS, 1941, 41 (2/3) :149-157

[9]

HASSTEDT SJ, 1983, AM J HUM GENET, V35, P1241

[10] SEGREGATION RATIOS IN ALPORTS SYNDROME [J].

MACNEILL, E ;

SHAW, RF .

JOURNAL OF MEDICAL GENETICS, 1973, 10 (01) :23-26

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