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An extended Family with a Dominantly Inherited Speech Disorder

✍ Scribed by Dr. J. A. Hurst; Dr. M. Baraitser; E. Auger; F. Graham; S. Norell


Book ID
115265646
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
269 KB
Volume
32
Category
Article
ISSN
0012-1622

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Cephalometric analysis of families with
✍ Murdoch-Kinch, Carol Anne; Bixler, David; Ward, Richard E. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 39 KB πŸ‘ 2 views

Crouzon syndrome (CS) is an autosomal dominant condition comprising orbital proptosis, midfacial hypoplasia, premature sutural synostosis, and altered proportions of bone lengths in the hands. In families the CS trait is highly variable. Several cases of affected sibs born to unaffected parents have