Response to Santavuori et al. regarding Walker‐Warburg syndrome and muscle‐eye‐brain disease

This publication has 8 references indexed in Scilit:

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• Identification of the Cystic Fibrosis Gene: Genetic Analysis
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• Congenital muscular dystrophy
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• Diagnostic criteria for Walker‐Warburg syndrome
  American Journal of Medical Genetics, 1989
• Muscle-eye-brain disease (MEB)
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• Smith‐Lemli‐Opitz syndrome‐type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality
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• Spectrum of anomalies in the Meckel syndrome, or: “Maybe there is a malformation syndrome with at least one constant anomaly”
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