Describing Crouzon and Pfeiffer syndrome based on principal component analysis.
暂无分享,去创建一个
F. Staal | A. Ponniah | F. Angullia | C. Ruff | M. Koudstaal | D. Dunaway
[1] J T Richtsmeier,et al. Comparative study of normal, Crouzon, and Apert craniofacial morphology using finite element scaling analysis. , 1987, American journal of physical anthropology.
[2] J. Posnick,et al. Craniofacial skeletal measurements based on computed tomography: Part II. Normal values and growth trends. , 1992, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
[3] J. Posnick,et al. Cranio-Orbito-Zygomatic Measurements from Standard CT Scans in Unoperated Crouzon and Apert Infants: Comparison with Normal Controls , 1992, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
[4] J. Posnick,et al. Crouzon syndrome: quantitative assessment of presenting deformity and surgical results based on CT scans. , 1993, Plastic and reconstructive surgery.
[5] M W Vannier,et al. Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes. , 1993, Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery.
[6] W. Reardon,et al. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes , 1995, Nature Genetics.
[7] E. Jabs,et al. FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing. , 1996, American journal of human genetics.
[8] U. Müller,et al. FGFR2 mutation in clinically nonclassifiable autosomal dominant craniosynostosis with pronounced phenotypic variation. , 1996, American journal of medical genetics.
[9] J T Richtsmeier,et al. Brief communication: a sample of pediatric skulls available for study. , 1997, American journal of physical anthropology.
[10] F. Bookstein. Shape and the information in medical images: a decade of the morphometric synthesis , 1997, Proceedings of the Workshop on Mathematical Methods in Biomedical Image Analysis.
[11] P. O’Higgins. The study of morphological variation in the hominid fossil record: biology, landmarks and geometry , 2000, Journal of anatomy.
[12] Eric Arnaud,et al. Management of craniosynostoses , 2000, Child's Nervous System.
[13] Jayesh Panchal,et al. Management of craniosynostosis. , 2003, Plastic and reconstructive surgery.
[14] R. Pfeiffer. Dominant erbliche Akrocephalosyndaktylie , 1964, Zeitschrift für Kinderheilkunde.
[15] R. Hennekam,et al. 3D analysis of facial morphology , 2004, American journal of medical genetics. Part A.
[16] F. Pezzetti,et al. Apert and Crouzon Syndromes: Clinical Findings, Genes and Extracellular Matrix , 2005, The Journal of craniofacial surgery.
[17] Christopher R Forrest,et al. International Anthropometric Study of Facial Morphology in Various Ethnic Groups/Races , 2005, The Journal of craniofacial surgery.
[18] J. Bonaventure,et al. Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome , 2006, European Journal of Human Genetics.
[19] C. Heike,et al. Syndromic craniosynostosis: from history to hydrogen bonds. , 2007, Orthodontics & craniofacial research.
[20] Clifford Ruff,et al. Using principal component analysis to describe the Apert skull deformity and simulate its correction. , 2012, Journal of plastic, reconstructive & aesthetic surgery : JPRAS.