Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.
Open Access
- 1 June 1969
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 6 (2), 113-120
- https://doi.org/10.1136/jmg.6.2.113
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Smith-Lemli-Opitz SyndromeAmerican Journal of Diseases of Children, 1968
- A familial syndrome of mental retardation in association with multiple congenital anomalies resembling the syndrome of Smith-Lemli-Opitz.1967
- The syndrome of retardation with urogenital and skeletal anomalies in siblingsThe Journal of Pediatrics, 1966
- A syndrome characterized by mental retardation, short stature, craniofacial dysplasia, and genital anomalies occurring in siblingsThe Journal of Pediatrics, 1966
- Dermatoglyphics in pediatric practiceThe Journal of Pediatrics, 1966
- A familial syndrome of facial and skeletal anomalies associated with genital abnormality in the male and normal genitals in the femaleThe Journal of Pediatrics, 1965
- A CASE OF SMITH-LEMLI-OPITZ SYNDROME OF MULTIPLE CONGENITAL ANOMALIES IN ASSOCIATION WITH DYSPLASIA EPIPHYSIALIS PUNCTATA1965
- A newly recognized syndromeof multiple congenital anomaliesThe Journal of Pediatrics, 1964
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960