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References

‘Markedly elevated neonatal IRT levels in the absence of CF gene mutations…’

 

 

Massie, Curnow et al
Arch Dis Child 2006; 91:222-225.

 

 

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Guidelines for Implementation of Cystic Fibrosis Newborn Screening Programs: Cystic Fibrosis Foundation Workshop Report

 

 

PEDIATRICS Vol. 119 No. 2 February 2007, pp. e495-e518

 

 

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New York State Cystic Fibrosis Consortium: The First 2.5 Years of Experience With Cystic Fibrosis Newborn Screening in an Ethnically Diverse Population

 

 

Robert Giusti, MDa, Ashley Badgwell, MSb, Alejandro D. Iglesias,

MDb,c and the New York State Cystic Fibrosis Newborn Screening

Consortium
PEDIATRICS Vol. 119 No. 2 February 2007, pp. e460-e467

 

 

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Cystic Fibrosis Diagnosed After 2 Months of Age Leads to Worse Outcomes and Requires More Therapy

 

 

Erika J. Sims, PhDa,b, Allan Clark, PhDb, Jonathan McCormick, MDc, Gita Mehta, MPhila, Gary Connett, FRCPCHd, Anil Mehta, FRCP(Edin)a on behalf of the United Kingdom Cystic Fibrosis Database Steering Committee
PEDIATRICS Vol. 119 No. 1 January 2007, pp. 19-28

 

 

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