## Abstract ## BACKGROUND: Pfeiffer syndrome (PS; OMIM #101600) is an autosomal dominant disorder characterized by craniosynostosis, midface hypoplasia, broad thumbs, brachydactyly, broad great toes, and variable syndactyly. ## CASE: We report a case of PS (type 3) with tracheal and visceral inv
β¦ LIBER β¦
Further evidence for an association between maternal smoking and craniosynostosis
β Scribed by Honein, Margaret A. ;Rasmussen, Sonja A.
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 29 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0040-3709
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