MeSH Review:
Facial Asymmetry
- Mutations of the TWIST gene in the Saethre-Chotzen syndrome. el Ghouzzi, V., Le Merrer, M., Perrin-Schmitt, F., Lajeunie, E., Benit, P., Renier, D., Bourgeois, P., Bolcato-Bellemin, A.L., Munnich, A., Bonaventure, J. Nat. Genet. (1997)
- Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations. Paznekas, W.A., Cunningham, M.L., Howard, T.D., Korf, B.R., Lipson, M.H., Grix, A.W., Feingold, M., Goldberg, R., Borochowitz, Z., Aleck, K., Mulliken, J., Yin, M., Jabs, E.W. Am. J. Hum. Genet. (1998)
- X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Cason, A.L., Ikeguchi, Y., Skinner, C., Wood, T.C., Holden, K.R., Lubs, H.A., Martinez, F., Simensen, R.J., Stevenson, R.E., Pegg, A.E., Schwartz, C.E. Eur. J. Hum. Genet. (2003)
- Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects. Wuyts, W., Waeber, G., Meinecke, P., Schüler, H., Goecke, T.O., Van Hul, W., Bartsch, O. Eur. J. Hum. Genet. (2004)
- Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32 leads to 13qter. Telfer, M.A., Clark, C.E., Casey, P.A., Cowell, H.R., Stroud, H.H. Clin. Genet. (1980)
- Distal 15q trisomy: phenotypic comparison of nine cases in an extended family. Schnatterly, P., Bono, K.L., Robinow, M., Wyandt, H.E., Kardon, N., Kelly, T.E. Am. J. Hum. Genet. (1984)
- Delayed speech development, facial asymmetry, strabismus, and transverse ear lobe creases: a new syndrome? Méhes, K. J. Med. Genet. (1993)
- Facial asymmetry, hippocampal pathology, and remote symptomatic seizures: a temporal lobe epileptic syndrome. Cascino, G.D., Luckstein, R.R., Sharbrough, F.W., Jack, C.R. Neurology (1993)
- Aicardi's syndrome; radiologic manifestations. Phillips, H.E., Carter, A.P., Kennedy, J.L., Rosman, N.P., O'Connor, J.F. Radiology. (1978)
- Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome. Joyce, C.A., Sharp, A., Walker, J.M., Bullman, H., Temple, I.K. Hum. Genet. (1999)
- Mandibular growth after distraction in patients under 48 months of age. Hollier, L.H., Kim, J.H., Grayson, B., McCarthy, J.G. Plast. Reconstr. Surg. (1999)
- Use of a miniaturized detector in facial bone scanning. Donoff, R.B., Jeffcoat, M.K., Kaplan, M.L. International journal of oral surgery. (1978)
- Relationship between transverse dental anomalies and skeletal asymmetry. Kusayama, M., Motohashi, N., Kuroda, T. American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics. (2003)
- Combined simultaneous distraction osteogenesis of the maxilla and mandible using a single distraction device in hemifacial microsomia. Vu, H.L., Panchal, J., Levine, N. The Journal of craniofacial surgery. (2001)
- Bilateral juvenile granulosa cell tumors in a 4-month-old dysmorphic infant. A clinical, histologic, and ultrastructural study. Pysher, T.J., Hitch, D.C., Krous, H.F. Am. J. Surg. Pathol. (1981)
- Progression of facial asymmetry in hemifacial microsomia. Kearns, G.J., Padwa, B.L., Mulliken, J.B., Kaban, L.B. Plast. Reconstr. Surg. (2000)
- Facial asymmetry: recognition of TMD. Steed, P.A. The Functional orthodontist. (1997)
- Facial asymmetries in hemifacial microsomia, Goldenhar syndrome, and Treacher Collins syndrome. Tiner, B.D., Quaroni, A.L. Atlas of the oral and maxillofacial surgery clinics of North America. (1996)
- Mandibular distraction osteogenesis using an intraoral device and bite plate for a case of hemifacial microsomia. Takashima, M., Kitai, N., Mori, Y., Murakami, S., Kreiborg, S., Takada, K. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. (2003)