Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency. [electronic resource]
Producer: 20000425Description: 973-81 p. digitalISSN:- 1073-449X
- Alleles
- DNA Mutational Analysis
- Female
- Frameshift Mutation
- Genetic Carrier Screening
- Homozygote
- Humans
- Infant, Newborn
- Lung -- pathology
- Male
- Polymorphism, Restriction Fragment Length
- Proteolipids -- genetics
- Pulmonary Surfactants -- genetics
- Respiratory Distress Syndrome, Newborn -- diagnosis
- Reverse Transcriptase Polymerase Chain Reaction
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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