Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation

J. Boyne; Steve Evans; Rodney J. Pollitt; Christopher J. Taylor; Ann Dalton

doi:10.1136/jmg.37.7.543

Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation

J. Boyne, Steve Evans, Rodney J. Pollitt, Christopher J. Taylor, Ann Dalton

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	543-547
Number of pages	5
Journal	Journal of Medical Genetics
Volume	37
Issue number	7
DOIs	https://doi.org/10.1136/jmg.37.7.543
Publication status	Published - 1 Jul 2000
Externally published	Yes

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title = "Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation",

author = "J. Boyne and Steve Evans and Pollitt, {Rodney J.} and Taylor, {Christopher J.} and Ann Dalton",

year = "2000",

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doi = "10.1136/jmg.37.7.543",

language = "English",

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journal = "Journal of Medical Genetics",

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T1 - Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation

AU - Boyne, J.

AU - Evans, Steve

AU - Pollitt, Rodney J.

AU - Taylor, Christopher J.

AU - Dalton, Ann

PY - 2000/7/1

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M3 - Letter

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JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

SN - 0022-2593

IS - 7

ER -

Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation

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