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Annals of Otology, Rhinology and Laryngology, 79, 194-202.","journal-title":"Annals of Otology, Rhinology and Laryngology"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"733","DOI":"10.1001\/archinte.1958.00260220049005","article-title":"A follow-up study of hereditary chronic nephritis","volume":"102","author":"Perkoff, G.T.; Nugent, Jr., C.A.; Dolowitz, D.A.; Stephens, F.E.; Carnes, W.H.; Tyler, F.H.","year":"1958","unstructured":"Perkoff, G. T., Nugent, C. A., Jr., Dolowitz, D. A., Stephens, F. E., Carnes, W. H., and Tyler, F. H. (1958). A follow-up study of hereditary chronic nephritis. Archives of Internal Medicine, 102, 733-746.","journal-title":"Archives of Internal Medicine"},{"key":"ref_11","first-page":"89","article-title":"Abnormal segregation in hereditary renal disease with deafness","volume":"13","author":"Shaw, R.F.; Glover, R.A.","year":"1961","unstructured":"Shaw, R. F. and Glover, R. A. (1961). Abnormal segregation in hereditary renal disease with deafness. American Journal of Human Genetics, 13, 89-97.","journal-title":"American Journal of Human Genetics"},{"key":"ref_12","series-title":"Proceedings of the Staff Meetings of the Mayo Clinic","first-page":"289","article-title":"Syndrome of hereditary hematuria, nephropathy and deafness","volume":"33","author":"Sturtz, G.S.; Burke, E.C.","year":"1958","unstructured":"Sturtz, G. S. and Burke, E. C. (1958). Syndrome of hereditary hematuria, nephropathy and deafness. Proceedings of the Staff Meetings of the Mayo Clinic, 33, 289-297."},{"key":"ref_13","first-page":"589","article-title":"Diagnostic value of serum complement determination in hereditary glomerulonephritis","volume":"65","author":"Wasserman, E.; Schwarz, F.; Wachstein, M.; Lange, K.","year":"1965","unstructured":"Wasserman, E., Schwarz, F., Wachstein, M., and Lange, K. (1965). Diagnostic value of serum complement determination in hereditary glomerulonephritis. Journal of Laboratory and Clinical Medicine, 65, 589-599.","journal-title":"Journal of Laboratory and Clinical Medicine"},{"key":"ref_14","article-title":"We strongly object to the diagnosis of craniofacial dysostosis (Crouzon syndrome) in the two sibs reported recently by Juberg and Chambers","volume-title":"Despite the shallow orbits present in both patients, the lack of proptosis rules out the Crouzon syndrome, which is characterized minimally by craniosynostosis, midface hypoplasia, and shallow orbits with secondary proptosis","author":"Sir","year":"1973","unstructured":"Sir, We strongly object to the diagnosis of craniofacial dysostosis (Crouzon syndrome) in the two sibs reported recently by Juberg and Chambers (1973). Despite the shallow orbits present in both patients, the lack of proptosis rules out the Crouzon syndrome, which is characterized minimally by craniosynostosis, midface hypoplasia, and shallow orbits with secondary proptosis (Cohen, 1973). Occasionally, craniosynostosis may even be absent, as in several affected family members reported by Shiller (1959)."},{"key":"ref_15","article-title":"The patients reported by Juberg and Chambers","volume-title":"represent an isolated form of craniosynostosis, consistent with autosomal recessive inheritance. One of us (M. M. C.) has also observed several instances of affected sibs with isolated craniosynostosis","year":"1973","unstructured":"The patients reported by Juberg and Chambers (1973) represent an isolated form of craniosynostosis, consistent with autosomal recessive inheritance. One of us (M.M.C.) has also observed several instances of affected sibs with isolated craniosynostosis."},{"key":"ref_16","unstructured":"An syndromes.","article-title":"An syndromes"},{"author":"Series","key":"ref_17","unstructured":"Series. (In press.)"},{"year":"1973","author":"Juberg, R.C.; Chambers, S.R.","key":"ref_18","unstructured":"Juberg, R. C. and Chambers, S. R. 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