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Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome
Background: Smith-Lemli-Opitz syndrome (MIM 270400) is an autosomal recessive malformation and mental retardation syndrome that ranges in clinical severity from minimal dysmorphism and mild mental retardation to severe congenital anomalies and intrauterine death. Smith-Lemli-Opitz syndrome is caused...
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| Hauptverfasser: | , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Group
2004
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735869/ https://ncbi.nlm.nih.gov/pubmed/15286151 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.018085 |
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