R. Nelson

发表

Growth Deficiency in Cystic Fibrosis Is Observable at Birth and Predictive of Early Pulmonary Function

C. Hodges, E. Damato, M. Decker, 2016, Biological research for nursing.

Association ofless cornmon cystic fibrosis mutations witha mildphenotypec

M. Porteous, A. Curtis, R. Nelson, 1991 .

Association of less cornmon cystic fibrosis mutations with a mild phenotypec

S. Bhattacharya, M. Porteous, J. Burn, 2022 .

phenotype . fibrosis mutations with a mild Association of less common cystic

M. Porteous, J. Burn, S. Bhattacharya, 2022 .

Association of less common cystic fibrosis mutations with a mild phenotype.

M. Porteous, J. Burn, S. Bhattacharya, 1991, Journal of medical genetics.

Sex ratio and heterozygote advantage in cystic fibrosis families.

R. Nelson, D. Pritchard, G. Hickman, 1983, Archives of disease in childhood.

Sexratio andheterozygote advantage incystic fibrosis families

R. Nelson, G. Hickman, 1983 .

Cystic fibrosis and coeliac disease : coexistence in two children

C. Anderson, M. Goodchild, R. Nelson, 2006 .

Lung transplantation for treatment of infants with surfactant protein B deficiency.

H. Colten, T. Spray, A. Hamvas, 1997, The Journal of pediatrics.

Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2

D. Bulman, A. Hahn, K. A. Scoggan, 2001, Journal of medical genetics.

Cystic fibrosis: what do patients know, and what else would they like to know?

R. Nelson, J. Beesley, A. Hames, 1991, Respiratory medicine.

Absence of cystic fibrosis mutations in a large Asian population sample and occurrence of a homozygous S549N mutation in an inbred Pakistani family.

S. Bhattacharya, R. Richardson, A. Curtis, 1993, Journal of medical genetics.

LAVAGE FOR INTESTINAL OBSTRUCTION IN CYSTIC FIBROSIS

D. Geddes, D. Stringer, G. Cleghorn, 1986, The Lancet.