Are the Mirhosseini‐Holmes‐Walton syndrome and the cohen syndrome identical?
- 1 October 1986
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 25 (2), 397-398
- https://doi.org/10.1002/ajmg.1320250227
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini‐Holmes‐Walton syndrome): Report of two patientsAmerican Journal of Medical Genetics, 1985
- Two brothers with Martsolf's syndrome.Journal of Medical Genetics, 1985
- Further delineation of the Cohen syndrome; report on chorioretinal dystrophy, leukopenia and consanguinityClinical Genetics, 1984
- Severe mental retardation, cataracts, short stature, and primary hypogonadism in two brothersAmerican Journal of Medical Genetics, 1978
- A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomaliesThe Journal of Pediatrics, 1973
- Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation.Journal of Medical Genetics, 1972