Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome
- 1 October 1983
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 141 (1) , 8-13
- https://doi.org/10.1007/bf00445661
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Rud Syndrome: Congenital Ichthyosis, Hypogonadism, Mental Retardation, Retinitis Pigmentosa and Hypertrophic PolyneuropathyNeuropediatrics, 1982
- Prenatal diagnosis of X-linked ichthyosisClinica Chimica Acta; International Journal of Clinical Chemistry, 1982
- Regional assignment of the gene locus for steroid sulfataseHuman Genetics, 1980
- Clinical and biochemical investigations on patients with partial deficiency of placental steroid sulfataseHuman Genetics, 1979
- X-linked ichthyosis, bilateral cryptorchidism, hypogenitalism and mental retardation in two siblingsClinical Genetics, 1976
- Congenital ichthyosis, mental retardation, dwarfism and renal impairment: A new syndromeClinical Genetics, 1975
- A syndrom characterized by congenital ichthyosis with atrophy, mental retardation, dwarfism, and generalized aminoaciduriaThe Journal of Pediatrics, 1973
- Lamellar Ichthyosis of the NewbornArchives of Dermatology, 1962
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"Archives of Dermatology, 1958
- ForwardActa Psychiatrica Scandinavica, 1957