Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter
- 1 December 1985
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 121 (12) , 1524-1528
- https://doi.org/10.1001/archderm.121.12.1524
Abstract
From JAMA Dermatology — Familial X-linked Ichthyosis, Steroid Sulfatase Deficiency, Mental Retardation, and Nullisomy for Xp223-pterThis publication has 10 references indexed in Scilit:
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- A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardationClinical Genetics, 1983
- Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidismEuropean Journal of Pediatrics, 1983
- X-Linked Ichthyosis: Increased Blood Cholesterol Sulfate and Electrophoretic Mobility of Low-Density LipoproteinScience, 1981
- INCREASED CHOLESTEROL SULFATE IN PLASMA AND RED BLOOD CELL MEMBRANES OF STEROID SULFATASE DEFICIENT PATIENTSJournal of Clinical Endocrinology & Metabolism, 1981
- Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man.Proceedings of the National Academy of Sciences, 1980
- Y-to-X chromosome translocation observed in two generationsHuman Genetics, 1980
- Regional assignment of the steroid sulfatase—X-linked ichthyosis locus: Implications for a noninactivated region on the short arm of human X chromosomeProceedings of the National Academy of Sciences, 1979
- Non-inactivation of an X-Chromosome Locus in ManScience, 1979
- X-LINKED ICHTHYOSIS DUE TO STEROID-SULPHATASE DEFICIENCYThe Lancet, 1978