Cystic fibrosis and heterozygote fitness

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Comment

. 1990 Dec 12;264(22):2867-8.

Comment

R B Johnson. JAMA. 1990.

. 1990 Dec 12;264(22):2867-8.

No abstract available

Comment on

The cystic fibrosis gene: medical and social implications for heterozygote detection.
Wilfond BS, Fost N. Wilfond BS, et al. JAMA. 1990 May 23-30;263(20):2777-83. JAMA. 1990. PMID: 2332921

Cystic fibrosis: a further case of an asymptomatic compound heterozygote.
White SM, Lucassen A, Norbury G. White SM, et al. Am J Med Genet. 2001 Nov 1;103(4):342-3. Am J Med Genet. 2001. PMID: 11746017 No abstract available.
Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosis.
Wilcken B. Wilcken B. J Paediatr Child Health. 2008 Apr;44(4):232-3; author reply 233. doi: 10.1111/j.1440-1754.2008.01293.x. J Paediatr Child Health. 2008. PMID: 18377372 No abstract available.
Cystic fibrosis (CF) is an autosomal recessive genetic disease.
Best RG, Mathis JN, Shah K, Golden R. Best RG, et al. J S C Med Assoc. 1994 Feb;90(2):78-9. J S C Med Assoc. 1994. PMID: 8170117 No abstract available.
[Progress in the analysis of cystic fibrosis: prenatal diagnosis and carrier detection].
Estivill X. Estivill X. Med Clin (Barc). 1989 Mar 18;92(10):375-7. Med Clin (Barc). 1989. PMID: 2565992 Review. Spanish. No abstract available.
Prenatal screening for cystic fibrosis: where are we now?
Farrell PM, Fost N. Farrell PM, et al. J Pediatr. 2002 Dec;141(6):758-63. doi: 10.1067/mpd.2002.127666. J Pediatr. 2002. PMID: 12461490 Review. No abstract available.