Severe cystic fibrosis phenotype in a delta F508/3272-26A-->G compound heterozygote. [electronic resource]
- Journal of medical genetics Nov 1995
- 919 p. digital
Publication Type: Case Reports; Comment; Letter
0022-2593
10.1136/jmg.32.11.919 doi
Child Cystic Fibrosis--genetics Cystic Fibrosis Transmembrane Conductance Regulator--genetics Fatal Outcome Heterozygote Humans Male Phenotype Point Mutation Sequence Deletion