HEREDITARY ALPHA1 - ANTITRYPSIN DEFICIENCY ASSOCIATED WITH CONGENITAL EXTRAHEPATIC BILE-DUCT HYPOPLASIA

被引：15

作者：

CHRISTEN, H

BAU, J

HALSBAND, H

机构：

[1] MED HSCH LUBECK,CHIRURG KLIN,LUBECK,FED REP GER

[2] MED HSCH LUBECK,KINDER KLIN & POLIKLIN,D-2400 LUBECK,FED REP GER

来源：

KLINISCHE WOCHENSCHRIFT | 1975年 / 53卷 / 02期

关键词：

D O I：

10.1007/BF01482714

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：90 / 91

页数：2

共 10 条

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FAGERHOL, M
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[J]. ACTA PAEDIATRICA SCANDINAVICA, 1972, 61 (06): : 632 - &
[2] BECKER W, 1968, Z KLIN CHEM CLIN BIO, V3, P113
[3] FAGERHOL MK, 1970, PROG MED GENET, V7, P96
[4] GEDDEDAHL T, 1972, ANN HUM GENET, V35, P393
[5] FAMILIAL EXTRAHEPATIC BILIARY ATRESIA
KRAUSS, AN
[J]. JOURNAL OF PEDIATRICS, 1964, 65 (6P1) : 933 - +
[6] HEREDITARY DEFICIENCY OF SERUM ALPHA1-ANTITRYPSIN
KUEPPERS, F
BEARN, AG
BRISCOE, WA
[J]. SCIENCE, 1964, 146 (365) : 1678 - &
[7] Landing B H, 1974, Prog Pediatr Surg, V6, P113
[8] MOORE TC, 1953, SURG GYNECOL OBSTET, V96, P215
[9] RUMLER W, 1961, ARCH KINDERHEILKD, V161, P238
[10] SHARP HL, 1969, J LAB CLIN MED, V73, P934