Prenatal diagnosis of genetic disorders of the skin by means of electron microscopy
- 1 January 1981
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 59 (4), 392-405
- https://doi.org/10.1007/bf00295479
Abstract
No abstract availableThis publication has 45 references indexed in Scilit:
- Prenatal diagnosis of harlequin ichthyosisClinical Genetics, 1980
- Regional Development of the Human Epidermis in the First Trimester Embryo and the Second Trimester Fetus (Ages Related to the Timing of Amniocentesis and Fetal Biopsy)Journal of Investigative Dermatology, 1980
- Prenatal Diagnosis of Congenital Bullous Ichthyosiform Erythroderma (Epidermolytic Hyperkeratosis) by Fetal Skin BiopsyNew England Journal of Medicine, 1980
- Zur Ultrastruktur der Epidermolysen mit junktionaler BlasenbildungDermatology, 1979
- X-linked icthyosis. A sulphatase deficiency.Archives of Disease in Childhood, 1978
- Electron Microscopy in the Early Diagnosis of Genetic Disorders of the SkinDermatology, 1978
- THE ROLE OF HUMAN SKIN COLLAGENASE IN EPIDERMOLYSIS BULLOSAJournal of Investigative Dermatology, 1977
- Epidermolysis bullosa hereditaria letalis. Clinical and histological manifestations and course of the diseaseArchives of Dermatology, 1974
- Ultrastructural distinction of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosisHuman Genetics, 1972
- Localization of the oxidative defect in phytanic acid degradation in patients with refsum's diseaseJournal of Clinical Investigation, 1969