Case report: Pulmonary hypoplasia and osteogenesis imperfecta type II with defective synthesis of alpha I(1) procollagen
- 1 January 1989
- Vol. 10 (3) , 165-171
- https://doi.org/10.1016/8756-3282(89)90049-5
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneityAmerican Journal of Medical Genetics, 1984
- Prenatal diagnosis of lethal perinatal osteogenesis imperfecta (OI Type II)The Journal of Pediatrics, 1982
- Reduced secretion of structurally abnormal type I procollagen in a form of osteogenesis imperfecta.Proceedings of the National Academy of Sciences, 1981
- Fetal lung hypoplasia: biochemical and structural variations and their possible significance.Archives of Disease in Childhood, 1981
- Protein fingerprinting by SDS-gel electrophoresis after partial fragmentation with CNBrAnalytical Biochemistry, 1979
- Genetic heterogeneity in osteogenesis imperfecta.Journal of Medical Genetics, 1979
- Primary Pulmonary HypoplasiaAmerican Journal of Diseases of Children, 1977
- Characterization of the Collagen Synthesized by Cultured Human Smooth Muscle Cells from Fetal and Adult AortaHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1977
- The estimation of two collagens from human dermis by interrupted gel electrophoresisBiochemical and Biophysical Research Communications, 1976
- The Number of Alveoli in the Terminal Respiratory Unit of Man During Late Intrauterine Life and ChildhoodArchives of Disease in Childhood, 1960