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注意:仅列出部分参考文献,下载原文获取全部文献信息。Genetics in Pulmonary Fibrosis-Familial Cases Provide Clues to the Pathogenesis of Idiopathic Pulmonary Fibrosis
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JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2007)
Adult-onset pulmonary fibrosis caused by mutations in telomerase
Kalliopi D. Tsakiri et al.
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Telomerase mutations in families with idiopathic pulmonary fibrosis
Mary Y. Armanios et al.
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The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome
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Incidence and prevalence of idiopathic pulmonary fibrosis
Ganesh Raghu et al.
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Gabriela M. Baerlocher et al.
NATURE PROTOCOLS (2006)
Clinical and pathologic features of familial interstitial pneumonia
MP Steele et al.
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HL Lee et al.
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Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF
WE Lawson et al.
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AU Wells et al.
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Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred
AQ Thomas et al.
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Nationwide prevalence of sporadic and familial idiopathic pulmonary fibrosis: evidence of founder effect among multiplex families in Finland
U Hodgson et al.
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Medical progress: Idiopathic pulmonary fibrosis.
TJ Gross et al.
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Adult familial cryptogenic fibrosing alveolitis in the United Kingdom
RP Marshall et al.
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