Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation.
Open Access
- 1 June 1972
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 9 (2), 193-196
- https://doi.org/10.1136/jmg.9.2.193
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Familial Syndrome of Primary Testicular Insufficiency with Normal Virilization, Blindness, Deafness and Metabolic AbnormalitiesNew England Journal of Medicine, 1969
- Radioimmunoassay of Human Follicle Stimulating and Luteinizing Hormones in Plasma1Journal of Clinical Endocrinology & Metabolism, 1968
- A SIMPLE SCREENING TEST FOR THE MARFAN SYNDROMEAmerican Journal of Roentgenology, 1966
- Chorioretinopathy With Hereditary MicrocephalyArchives of Ophthalmology (1950), 1966
- The Metacarpal IndexArchives of Internal Medicine, 1964
- Laurence-Moon-Biedl SyndromeAmerican Journal of Diseases of Children, 1961
- Familial Spastic Paraplegia with Amyotrophy, Oligophrenia, and Central Retinal DegenerationArchives of Neurology, 1959
- Retinitis pigmentosa combined with congenital deafness; with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: A clinical and genetico-statistical study.1959
- RAPID MICRO-MODIFICATION OF THE ZIMMERMANN/CALLOW PROCEDURE FOR THE DETERMINATION OF 17-KETOSTEROIDS IN URINEActa Endocrinologica, 1951
- The Laurence-Moon-Biedl syndrome. Report of a typical case with complete necropsy.1951