A clinical study of the craniofacial features in Apert syndromeCOHEN, M. M; KREIBORG, S.International journal of oral and maxillofacial surgery. 1996, Vol 25, Num 1, pp 45-53, issn 0901-5027Article

Germinal mosaicism in Crouzon syndrome : a family with three affected siblings of normal parentsNAVARRETE, C; PENA, R; PENALOZA, R et al.Clinical genetics. 1991, Vol 40, Num 1, pp 29-34, issn 0009-9163Article

Cytogenetic analyses on patients with Crouzon's and Apert's syndromesMARK, J; LILJA, J; STENMAN, G et al.Hereditas (Landskrona). 1986, Vol 105, Num 1, pp 157-159, issn 0018-0661Article

A severe form of Crouzon's disease : Clinical and radiological correlationABDALLAH, A. M; NELSON, L. B.Journal of pediatric ophthalmology and strabismus. 1998, Vol 35, Num 4, pp 230-231, issn 0191-3913Article

Two craniosynostotic syndrome Loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26XIANG LI; FELDMAN LEWANDA, A; JONES, M. C et al.Genomics (San Diego, Calif.). 1994, Vol 22, Num 2, pp 418-424, issn 0888-7543Article

FGFR2 exon IIIa and III c mutations in Crouzon, Jackson-Weiss, and pfeiffer syndromes : Evidence for missense changes, insertions, and a deletion due to alternative RNA splicingMEYERS, G. A; DAY, D; SCOTT, A. F et al.American journal of human genetics. 1996, Vol 58, Num 3, pp 491-498, issn 0002-9297Article

Surgical correction of Crouzon syndromeDAVID, D. J; SHEEN, R.Plastic and reconstructive surgery (1963). 1990, Vol 85, Num 3, pp 344-354, issn 0032-1052, 11 p.Article

Hydrocephalus in Crouzon's syndromeHANIEH, A; SHEEN, R; DAVID, D. J et al.Child's nervous system (Print). 1989, Vol 5, Num 3, pp 188-189, issn 0256-7040Article

Luxation of the globe and Crouzon's disease : The first reported case in SingaporeLIM, L; WONG, P. K.Singapore medical journal. 1996, Vol 37, Num 5, pp 553-555, issn 0037-5675Article

Airway obstruction in the Crouzon syndrome : case report and review of the literatureSIROTNAK, J; BRODSKY, L; PIZZUTO, M et al.International journal of pediatric otorhinolaryngology. 1995, Vol 31, Num 2-3, pp 235-246, issn 0165-5876Article

Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndromOLDRIDGE, M; WILKIE, A. O. M; MALCOLM, S et al.Human molecular genetics (Print). 1995, Vol 4, Num 6, pp 1077-1082, issn 0964-6906Article

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeREARDON, W; WINTER, R. M; RUTLAND, P et al.Nature genetics. 1994, Vol 8, Num 1, pp 98-103, issn 1061-4036Article

Sonographic appearance of craniofacial dysostosis (Crouzon syndrome) in the second trimesterGOLLIN, Y. G; ABUHAMAD, A. Z; INATI, M. N et al.Journal of ultrasound in medicine. 1993, Vol 12, Num 10, pp 625-628, issn 0278-4297Article

Cloverleaf skull : a severe form of Crouzon's syndrome : a new concept in aetiologyROHATGI, M.Acta neurochirurgica. 1991, Vol 108, Num 1-2, pp 45-52, issn 0001-6268, 8 p.Article

Courzon syndrome : prenatal ultrasound diagnosis by binocular diametersLEO, M. V; SUSLAK, L; GANESH, V. L et al.Obstetrics and gynecology (New York. 1953). 1991, Vol 78, Num 5, pp 906-908, issn 0029-7844, 2Article

Spontaneous mutation and parental age in humansRISCH, N; REICH, E. W; WISHNICK, M. M et al.American journal of human genetics. 1987, Vol 41, Num 2, pp 218-248, issn 0002-9297Article

A Crouzon syndrome synonymous mutation activates a 5' splice site within the IIIC exon of the FGFR2 geneDEL GATTO, F; BREATHNACH, R.Genomics (San Diego, Calif.). 1995, Vol 27, Num 3, pp 558-559, issn 0888-7543Article

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10PRESTON, R. A; POST, J. C; MULVIHILL, J. J et al.Nature genetics. 1994, Vol 7, Num 2, pp 149-153, issn 1061-4036Article

Crouzon syndrome: cephalometric analysis and evaluation of pathogenesisCARINCI, F; AVANTAGGIATO, A; CURIONI, C et al.The Cleft palate-craniofacial journal. 1994, Vol 31, Num 3, pp 201-209, issn 1055-6656Article

Jackson-Weiss syndrome registered in four successive generations. The facies of Crouzon's syndrome with foot abnormalitiesSTANKOVIC, B; KRSTIC, V; STANKOV, B et al.Documenta ophthalmologica. 1994, Vol 85, Num 3, pp 281-286, issn 0012-4486Article

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2JABS, E. W; XIANG LI; SCOTT, A. F et al.Nature genetics. 1994, Vol 8, Num 3, pp 275-279, issn 1061-4036Article

Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromesKREIBORG, S; MARSH, J. L; COHEN, M. M et al.Journal of cranio-maxillo-facial surgery. 1993, Vol 21, Num 5, pp 181-188, issn 1010-5182Article

A modified occlusal splint to avoid tracheotomy for total midface osteotomiesPOSNICK, J. C; NAKANO, P; TAYLOR, M et al.Annals of plastic surgery. 1992, Vol 29, Num 3, pp 223-230, issn 0148-7043Article

Birth prevalence studies of the Crouzon syndrome : comparison of direct and indirect methodsCOHEN, M. M; KREIBORG, S.Clinical genetics. 1992, Vol 41, Num 1, pp 12-15, issn 0009-9163Article

Cervical spine in the apert syndromeKREIBORG, S; BARR, M. JR; MICHAEL COHEN, M. JR et al.American journal of medical genetics. 1992, Vol 43, Num 4, pp 704-708, issn 0148-7299Article