PULMONARY-FUNCTION IN OBLIGATE HETEROZYGOTES FOR CYSTIC-FIBROSIS

被引：7

作者：

BYARD, PJ

DAVIS, PB

机构：

[1] CASE WESTERN RESERVE UNIV,RAINBOW BABIES & CHILDRENS HOSP,SCH MED,DEPT PEDIAT,CLEVELAND,OH 44106

[2] CASE WESTERN RESERVE UNIV,RAINBOW BABIES & CHILDRENS HOSP,SCH MED,DEPT MED,CLEVELAND,OH 44106

[3] CASE WESTERN RESERVE UNIV,RAINBOW BABIES & CHILDRENS HOSP,SCH MED,DEPT EPIDEMIOL & BIOSTAT,CLEVELAND,OH 44106

来源：

AMERICAN REVIEW OF RESPIRATORY DISEASE | 1988年 / 138卷 / 02期

关键词：

D O I：

10.1164/ajrccm/138.2.312

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

引用

页码：312 / 316

页数：5

共 27 条

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[7] DIAGNOSIS AND TREATMENT OF CYSTIC-FIBROSIS - AN UPDATE [J].

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CHEST, 1984, 85 (06) :802-809

[8]

DAVIS PB, 1984, AM REV RESPIR DIS, V129, P911

[9] PULMONARY ABNORMALITIES IN OBLIGATE HETEROZYGOTES FOR CYSTIC-FIBROSIS [J].

DAVIS, PB ;

VARGO, K .

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[10]

DAVIS PB, 1987, AM REV RESPIR SA464, V135

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