Pulmonary abnormalities in obligate heterozygotes for cystic fibrosis.

Author:

Davis P B,Vargo K

Publisher

BMJ

Subject

Pulmonary and Respiratory Medicine

Reference21 articles.

1. The eccrine sweat defect in cystic fibrosis of the pancreas (mucoviscidosis);PA, Di Sant'Agnese; GF, Powell;Ann NY Acad Sci

2. A comparison of sweat chlorides and intestinal fat absorption in chronic obstructive pulmonary emphysema and fibrocystic disease of the pancreas;Wood, J.A.; Fishman, A.P.; Reemtsma, K.; Barker, H.G.; di Sant'Agnese, P.A.;N Engl J Med,1959

3. Absence of detrimental effect of the carrier state for the cystic fibrosis gene;Hallett, W.Y.; Knudson, A.G.; Massey, F.J.;Am Rev Respir Dis,1965

4. Observations on (i) sweat sodium levels in relation to chronic respiratory disease in adults and (ii) the incidence of respiratory and other disease in parents and siblings of patients with fibrocystic disease of;Anderson, C.M.; Freeman, M.; Allan, J.; Hubbard, L.;the pancreas. Med J Aust,1962

5. The prevalence of respiratory disease in heterozygotes for the gene for fibrocystic disease of the pancreas;Batten, J.; Muir, D.; Simon, G.; Carter, C.;Lancet,1963

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