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- Jackson-Weiss Syndrome OMIM
Jackson et al. (1976) reported a syndrome of craniosynostosis, midfacial hypoplasia, and foot anomalies in an Amish kindred. - Fibroblast growth factor receptor mutations and craniosynostosis:...
...in three of the best known craniosynostosis syndromes, namely Apert, Crouzon and Pfeiffer syndromes, as well as in Jackson-Weiss syndrome and... - What is Jackson Weiss Syndrome
...link What is Jackson-Weiss syndrome? Jackson-Weiss syndrome is a genetic disorder characterized by ... bones of the skull (craniosynostosis),... - Molecular and cellular bases of syndromic craniosynostoses.
...the clinical condition of 'craniosynostosis', a ... conditions including Apert, Pfeiffer, Crouzon, Beare-Stevenson and Jackson-Weiss syndromes.