Pages that link to "Pfeiffer syndrome"
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The following pages link to Pfeiffer syndrome:
Displayed 32 items.
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- Pfeiffer Syndrome (redirect page) (← links)
- Acrocephalosyndactyly, Type V (redirect page) (← links)
- Craniosynostosis (← links)
- Autosomal recessive (← links)
- List of diseases (P) (← links)
- List of genetic disorders (← links)
- Saethre-Chotzen syndrome (← links)
- Apert syndrome (← links)
- Fibroblast growth factor receptor 2 (← links)
- Chromosome 10 (human) (← links)
- Chromosome 8 (human) (← links)
- Dominance relationship (← links)
- Fibroblast growth factor receptor 1 (← links)
- Webbed toes (← links)
- Hearing loss with craniofacial syndromes (← links)
- Testpage3 (← links)
- Recessive gene (← links)
- Acrocephalosyndactyly, type V (redirect page) (← links)
- Chromosome 8 (← links)
- Chromosome 10 (← links)
- Antley-Bixler syndrome (← links)
- Acrocephalosyndactylia (← links)
- Overgrowth syndrome (← links)
- Collagen disease (← links)
- Congenital heart disease causes (← links)
- Craniosynostosis (patient information) (← links)
- Exophthalmos causes (← links)
- Hearing impairment causes (← links)
- Sandbox:Mental retardation causes (← links)
- Template:Multiple abnormalities (← links)