Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance
- PMID: 4389828
- PMCID: PMC1468850
- DOI: 10.1136/jmg.6.2.113
Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance
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