Publication:
Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis [3]

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dc.contributor.authorIris Schrijveren_US
dc.contributor.authorWikrom Karnsakulen_US
dc.contributor.authorChanin Limwongseen_US
dc.contributor.authorSudha Ramalingamen_US
dc.contributor.authorRamalingam Sankaranen_US
dc.contributor.authorPhyllis Gardneren_US
dc.contributor.authorRichard Mossen_US
dc.contributor.otherStanford University Medical Centeren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-21T08:30:16Z
dc.date.available2018-06-21T08:30:16Z
dc.date.issued2005-02-15en_US
dc.identifier.citationAmerican Journal of Medical Genetics. Vol.133 A, No.1 (2005), 103-105en_US
dc.identifier.doi10.1002/ajmg.a.30472en_US
dc.identifier.issn15524825en_US
dc.identifier.other2-s2.0-12944291462en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/17063
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=12944291462&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleNovel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis [3]en_US
dc.typeLetteren_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=12944291462&origin=inwarden_US

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